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The PNNL zinc-polyiodide flow battery reduces the battery's size and cost and makes it well suited to store energy in densely populated cities and provides a battery that packs far more energy than any other battery of its kind and size. The zinc-polyiodide redox flow battery, described in Nature Communications, uses an electrolyte that has more than two times the energy density of the next-best flow battery used to store renewable energy and support the power grid. The energy density is approaching that of a type of lithium-ion battery used to power portable electronic devices and some small electric vehicles. "With improved energy density and inherent fire safety, flow batteries could provide long-duration energy storage for the tight confines of urban settings, where space is at a premium," said Imre Gyuk, energy storage program manager at the Department of Energy's Office of Electricity Delivery and Energy Reliability, which funded this research. "This would enhance the resiliency and flexibility of the local electrical grid." "Another, unexpected bonus of this electrolyte's high energy density is it could potentially expand the use of flow batteries into mobile applications such as powering trains and cars," said the study's corresponding author, Wei Wang, a materials scientist at PNNL. Both flow and lithium-ion batteries were invented in the 1970s, but only the lithium-ion variety took off at that time. Lithium-ion batteries could carry much more energy in a smaller space than flow batteries, making them more versatile. As a result, lithium-ion batteries have been used to power portable electronics for many years. And utilities have begun using them to store the increasing amounts of renewable energy generated at wind farms and solar power facilities. But the high-energy lithium-ion batteries' packaging can make them prone to overheating and catching fire. Flow batteries, on the other hand, store their active chemicals separately until power is needed, greatly reducing safety concerns. This feature has prompted researchers and developers to
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There are many problems and health safety issues when dust and/or debris is present in an environment such as construction and agricultural environments. As heavy machinery moves over unpaved roads and construction and agricultural sites, dust may be thrown into the atmosphere. Such dust may pose both health and economic risks to construction workers, farmers and others near these environments. Such risks may come from two sources, among others: suspended dust drying out the atmosphere around the site and from the inhalation of dust. The drying of the atmosphere from the suspended dust particles may lead to rapid dehydration of individuals, which can lead to heat stroke, sluggishness, hallucinations, and a variety of other physical and psychological ailments. Airborne crystalline silica that originates from the earth, concrete, masonry and rock on a site may become lodged in the membranes and/or lungs of the respiratory systems of the people on and near the site. Once there, they may harden and cause permanent damage and even death. Economic risks may be a consequence of the health risks and from loss of productivity of the land. Dehydration may lead to loss in productivity. Workers may need more breaks to replenish fluids, may be less productive because they are uncomfortable, and may be less energetic, which leads to less work being accomplished per unit time. Longer term health issues may lead to loss of skilled workers and may increase the risk of lawsuits. Additionally, dust may lead to loss of moisture from plants and animals. In turn, more water may be consumed in agricultural processes. Dust may also lead to loss of topsoils (e.g., soils which may contain the most minerals and nutrients for productive plant growth). Loss of water from soil may lead to crop failure and failure to retain water in the soil may lead to greater water consumption, as water may be needed to be constantly applied. Previous solutions to these problems have included the constant application of water to sites using tanker trucks, fire hydrants and/or hoses. However, in such solutions, the water evaporates quickly, as it is not retained. This may lead to resumption of dust kick up into the atmosphere. Thus, water must be constantly applied. However, too much water at any given time may lead to muddy conditions. Oils have been used to suppress dust, but such oils are difficult to clean and are generally irreversible. Polymers and emulsions such as latex rubber and poly(vinyl acetate/vinyl alcohol) have been used as a fixation media but lack biodegradability and do not retain water. These polymers are generally used at a high concentration, and tend to bind soil, gravel and/or rocks together into large clumps. Under certain conditions (such in helicopter landing environments) large clumps of material may be thrown through the air, causing a safety hazard.
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It's been more than 50 years since John Gurdon first placed a nucleus from a differentiated cell of a Xenopus laevis tadpole into an enucleated Xenopus egg and regenerated a complete animal. This demonstrated two important facts: the somatic cell nucleus contains the complete genetic information needed for the production of the organism, and nuclei of differentiated cells can be reprogrammed into an embryonic state by the egg cytoplasm. Nowadays, this remarkable feat of reprogramming to generate a whole animal is almost commonplace, with Dolly the sheep being perhaps the most famous example. We now know that in some species reprogramming of nuclei in differentiated tissue can be achieved (albeit at low efficiency) by as few as four protein factors. And we know that the egg cytoplasm of some mammals can reprogram the mature nuclei of closely related species to the extent that live animals can be obtained (in the case of cow and gaur, for instance), while reprogramming of cells from more widely diverged species is only partially successful. What we don't know is why—and at what stage—divergent species reprogramming fails? In research reported in this issue of PLoS Biology, Narbonne, Simpson, and Gurdon tackled this problem using two frog species—X. laevis and Xenopus tropicalis—separated by more than 60 million years of evolution. They show that the failure to reprogram distantly related species may arise from a small suite of factors rather than from a systemic failure, suggesting a strategy for overcoming this longstanding developmental mystery. To approach this problem, the researchers inactivated the resident nucleus of eggs with ultraviolet light and fertilized them with sperm from one or the other species. When sperm and egg were from the same species, viable haploid tadpoles developed, showing that sperm nuclei can be correctly reprogrammed by the egg cytoplasm. In contrast, when sperm and egg came from the diverged species—that is, when inactivated X. laevis eggs were fertilized with X. tropicalis nuclei—they failed to develop properly. Despite active cell division, the embryos stalled around a stage known as gastrulation. This failure could result from some defect in nuclear reprogramming, or it might result from an incompatibility between the two species. For example, the “foreign” nucleus could interfere with the normal function of the host cytoplasm. An important stage in somatic nuclear reprogramming is embryonic gene activation (EGA), when new embryo-specific gene transcripts and new embryonic proteins from the mature nucleus are produced. The researchers found, at least in a limited sampling, that this stage seemed to proceed normally for the foreign nucleus and host egg species (although the authors acknowledge that a wider sampling might have revealed differences). Another obvious question is whether the foreign nucleus can cooperate with the mitochondria of the foreign cytoplasm. Mitochondria produce the energy currency of the cell—ATP—and have their own genomes, which produce some of the proteins needed for ATP generation; the nucleus encodes the remaining proteins. It's possible that millions of years of evolution and species divergence produced an incompatibility between the host mitochondria and the new nucleus, resulting in energy deficiency. Again, this did not seem to be the case (although ATP is not the only mitochondrial product that requires nucleus and cytoplasm cooperation; precursors for fats are also produced in the mitochondria). The researchers found another potential point of developmental failure for the cross-species hybrids: the hybrid embryos didn't seem to organize properly to form the long axis, which is critical for normal development. This could result from a failure to produce the signaling molecules that normally produce cell elongation or from a failure to read such signals. The answer seems to be a bit of both, as explants of the hybrid embryos elongate better when conjoined to parts of non-hybrid embryos, and non-hybrids do not elongate as well when attached to hybrids. Thus, a failure to produce and respond to elongation-signaling molecules offers a partial explanation. The authors noted that the hybrid embryos seemed to be relatively short of Xbra, a protein that regulates gene expression and is known to be important for convergence extension. By up-regulating Xbra expression in hybrid embryos, they could improve embryo elongation. Taken altogether, these results suggest that divergent species hybrids may fail as a result of a limited number of deficiencies—which, on a positive note, could conceivably be overcome by modulation of relatively few factors—rather than arising from gross failures of universal processes such as embryonic gene expression or energy metabolism. Why should we care about hybridization between divergent species? One day, it might be possible to enlist hybridization to develop a surrogate breeding system using differentiated cells of endangered or even extinct animals and eggs from a more readily available animal. Somatic cell nuclear reprogramming and development in a surrogate cytoplasm might also provide a better and more acceptable source of embryonic stem cells for therapy than current methods. But at the most basic level, understanding the mechanisms that lead to reproductive isolation helps us understand how species diverge over evolutionary time.
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Many computer-related applications incorporate some level of security to restrict user access. For example, in many applications, it is often necessary that a user of a computer provide a password to log on to a computer and corresponding network. The use of a password provided by a user affords at least some level of protection against intruders that would otherwise tamper with a computer and its contents. Although the use of a password can be advantageously incorporated in many applications, there are sometimes drawbacks associated with their use. For instance, a user can forget a password if it is not used for an extended period of time. In some cases, a user can forget his or her password after returning from a long vacation. To make matters worse, some systems require a user to change the password on a periodic basis for heightened security. This only adds to the difficulty of keeping track of a password at any given time. Even if a password is written on a piece of paper for later reference, the paper can be easily lost or destroyed, thwarting its purpose. A password is also easily replicated to the extent that it can be transferred from one person to another by word of mouth. Thus, if a hacker breaks into a computer system and retrieves a user's password, this key is easily passed on to other vandals who can then tamper with a computer system and its contents. Moreover, a user that is assigned a password can misplace his or her trust in a friend who carelessly reveals a password to others even though it was intended to be kept secret. These potential drawbacks are particularly disturbing since a corporation's most valuable asset is quite often information accessible by a user logging onto a password-protected computer.
3.03125
3
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Thursday, July 20, 2017 Let's Learn Sinhalese in English 4 Now let’s learn how to express something that is going to happen in the future (that is, construction of the future tense sentences). There are mainly four ways. We will consider all forms (like negative statement, questions, etc) of the same sentence. There is nothing to learn anew in the first method. Actually, you can use the same present time sentence you have been learning so far here. Usually you use an adverb (like tomorrow) that denotes future with that too (it’s not required though). Stephanie heta e:ka kiyanava: . (Stephanie will tell it tomorrow.) Api anidhdha: yanava: . (We will go day after tomorrow.) Egollo e:ka karanava: . (They will do it.) The negative statement form is just the same negative statement that you have already learned. There is another popular way of expressing something in future (the second method). In that sentence pattern, you just change the ending of “-nava:” verb. To construct this future tense verb, you first remove the “-nava:” part, and you append “-a:vi”. Balanava: → Balanava: + a:vi → Bala:vi (will look) Karanava: → Kararanava: + a:vi → Kara:vi (will do) Now you can make future tense sentences as follows. Shane ya:vi. (Shane will go.) Ayda bath uya:vi. (Ayda will cook rice.) Gasa kapa:vi. (The tree will be cut.) However, this form of future tense is not used with a subject of I or We (first person pronouns). If you use this form of verb with I or We, that would be a future time sentence of course, but additionally that sentence will mean an indefinite expression (uncertain whether or not the action will be done). In short, such a sentence is expressed in English with the helping verbs of “may, might”. Man ya:vi. (I may go. / I will probably go.) Api e:ka kara:vi. (We may do it. / We will probably do it.) Surprisingly, if you want to express an indefinite future tense (just as discussed in the previous paragraph) with any subject (in addition to I and We), we use this same sentence. So, this sentence pattern has two meanings with any noun/subject other than I, We – one is “normal future tense”, and the other is “indefinite future tense”. Eya: ya:vi. (He will probably go. / He may go.) Natalie e:vi. (Natalie may come. / Natalie will probably come.) Oya: e:ka kiya:vi. (You may tell it. / You will probably tell it.) The negative statement of this second kind of future tense pattern is as same as the normal negative statement you already know. Shane yanne naehae. (Shane will not go.) (remember this same sentence has the meaning of “Shane does not go” and “Shane is not going”; take the correct meaning based on the context) Ayda bath uyanne naehae. (Ayda will not cook rice.) (also, “Ayda does not cook rice” and “Ayda is not cooking rice”) To form the positive question, you just add “-dha” at the end of the verb of the positive statement as follows. This question form also applies to the indefinite future tense. Shane ya:vidha? (Will Shane go? Or May Shane go?) Ayda bath uya:vidha? (Will Ayda cook rice? Or May Ayda cook rice?) There is another popular way to construct the negative question. It is formed like this. First assume that “-nava:” verb form is there; now remove “va:” from that "assumed" verb. After that, you put “ekak naehae” at the end. This also applies to the indefinite future tense. See how it is done below. The third method is exclusive for the subject of I or We (first person pronouns). It is similar to English “shall” sentences. Here, the “-nava:” ending of the verb is changed to “-nnam”. Mama yanava: . → Mama yannam. (I shall go.) Api e:ka kohomahari karannam. (We shall do it somehow or other.) The negative statement of this type of sentence is as same as normal negative statement. Mama yanne naehae. (I shall not go.) Api e:ka karanne naehae. (We shall not do it.) This is how we construct the positive question. You remove “m” from the verb (let’s call this verb participle “nna verb” from this moment on), and append “dha”. Actually, this is how we make request in Sinhala too. Karannam → Karannam + dha = karannadha Mama yannadha? (Shall I go?) Api e:ka karannadha? (Shall we do it?) Last let’s make the negative question. First remove “m” from the verb like we did earlier (that is, make the “nna verb”), and put “epa:dha” after that. Karannam → Karannam epa:dha = karanna epa:dha Mama yanna epa:dha? (Shall I not go?) Api e:ka karanna epa:dha? (Shall we not do it?) The fourth method of making a future tense is similar to “be going to” sentence pattern in English. Here, we use the “nna verb” and after that we put “yanne” or “yanava:”. Mama potha kiyavanna yanne/yanava: . (I am going to read the book.) Eya: nidiyanna yanava:/yanne. (She/He is going to sleep.) If you substitute “inne” or “innava:” for “yanne” or “yanava:” in the above sentence pattern, then you change the meaning from “be going to” to “be planning to” or “be about to”. It also gives kind of future meaning. Mama potha kiyavanna inne/innava: . (I am planning to read the book. / I am about to read the book.) Eya: nidyanna inne/innava: . (He/She is planning to sleep.) Let’s make commands in Sinhala now. It’s very easy. Always the command is directed to the person in your presence (that is, “you”). It’s the same as in English. Follow the normal Sinhala sentence order. Here, the doer is “oya:” (singular) or “o:gollo/o:gollan, oya:la:” (plural) subject. You can omit it if you like (as in English). There is a small change in the verb ending; you just put the “nna verb” instead of the normal “-nava: verb” form. Oya: yanna. (You go.) Yanna. (Go.) Oya: bath ho’mdin kanna. (You eat rice well.) Bath kanna. (Eat rice.) Ogollo loku potha kiyavanna. (You (plural) read the big book.) Potha kiyavanna. (Read the book.) To give a command not to do something, you just put “epa:” after verb, or before the subject (if existing), or after the subject (whether or not it exists). Oya: yanna epa: . Epa: oya: yanna. Oya: epa: yanna. (You don’t go.) Yanna epa: . Epa: yanna. (Don’t go.) Oya: bath kanna epa: . Epa: oya: bath kanna. Oya epa: bath kanna. (You don’t eat rice.) Bath kanna epa: . Epa: bath kanna. (Don’t eat rice.) Ogollan potha kiyavanna epa: . Epa: ogollan potha kiyavanna. Ogollan epa: potha kiyavanna. (You don’t read the book.) Potha kiyavanna epa: . Epa: potha kiyavanna. (Don’t read the book.) If you want to make the command more polite, you can put “karuna:karala” (please) at the beginning or the end of the command. Karuna:karala oya: yanna. Oya: yanna karuna:karala. (You go please.) Karuna:karala yanna Yanna karuna:karala. (Go please.) Karuna:karala oya: yanna epa: . / Oya: yanna epa: karuna:karala. Karuna:karala epa: oya: yanna. / Epa: oya: yanna karuna:karala. Karuna:karala oya: epa: yanna. / Oya: epa: yanna karuna:karala. (You don’t go please.) Karuna:karala yanna epa: . / Yanna epa: karuna:karala. Karuna:karala epa: yanna. / Epa: yanna karuna:karala. (Don’t go please.) If you like, you can substitute “please” for “karuna:karala” too. For example, Please oya: yanna. / Oya: yanna please. (Please go.) Please yanna epa: . / Yanna epa: please. (Please don’t go.) You can make the command milder. And it probably can be considered as a plead now (instead of a command). For that, you append “-ko” to the “nna verb”. You may include “please” or “karuna:karala” to make it “much milder”. There is no negative form of this. Oya: yannako. Yannako oya: Yannako. (Go. Will you?) You can also make the command stronger/stringent. You specially use this form of command when you are mad at somebody (or scolding somebody or in a quarrel, etc). You never use this form of command at your parents, older relatives, teachers, honorable people, etc. It’s harsh. To make this harsh command, you put a verb made as follows (you remove the “nava:” from the “nava: verb” form, and append “pan” to it). No negative form of this exists. Karanava: → Karanava: + pan = Karapan Potha liyapan. (Read the book.) Surprisingly, this same command form is used among friends too. Then it has no harsh meaning, but instead it gets a friendly meaning. Only in this "friendly" situation, you may add “please” or “karuna:karala” to this "-pan" type command.
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Introduction ============ Bacterial diseases represent some recalcitrance and difficulties to manage the pest problems affecting commercial vegetable production. Spraying with antibiotics and pesticides, usually suggested controlling bacterial diseases, have never been satisfactory. Antibiotics and synthetic pesticides are forbidden in many countries because of their exerting a negative impact such as high and acute toxicity, long degradation periods and accumulation in the food chain. Therefore, losses from bacterial diseases can be substantial all over the world. Plant diseases caused by bacteria are factors in several plant family members (Aktar et al., 2009\[[@R1]\]). In addition; bacterial diseases caused by pathovars of *Xanthomonas* also result in a decreased yield of harvest. Pathovars of *Xanthomonas* are reported to have developed resistance to several antibiotics such as kanamycin, ampicillin, penicillin, and streptomycin (Rodriguez et al., 1997\[[@R18]\]). This seriously hinders the management of diseases of crops and agricultural products (Satish et al., 1999\[[@R19]\]). Besides, control of the disease is difficult, often requiring expensive and complex integrated pest management (IPM), including the use of contamination-free seeds, sanitization practices, and the use of chemicals (Araujo et al., 2003\[[@R2]\]). Naturally occurring biologically active plant products such as plant-based essential oils and organic extracts, pure compounds could be a source of new eco-friendly pesticides to serve as templates for new and more effective compounds in controlling plant pathogenic microorganisms. Furthermore, bio-pesticides have been suggested as effective substitutes for chemical pesticides (Gan-Mor and Matthews, 2003\[[@R9]\]). *Poncirus trifoliata*Rafin (Rutaceae), also known as trifoliate orange, is a close relative to the *Citrus*trees. It is a decidious or semi-decidious shrub, a native of China and Korea, and is also known as the Korean bitter orange. Traditionally, trifoliata oranges (*P. trifoliata*) have been widely used in folk medicine as a remedy for gastritis, dysentery, inflammation, digestive ulcers, etc. A scientific investigation into the health-maintaining properties of trifoliate orange fruit has revealed its anti-inflammatory, antibacterial and anti-anaphylactic activities (Kim et al., 1999\[[@R11]\]). In Korea, fruit extracts of *P. trifoliate* are used in some over-the-counter drugs for the treatment of a variety of gastrointestinal (GI) disorders (Lee et al., 2005\[[@R13]\]). Another researcher reported that poncirus fruit is a potent antileukaemic agent by promoting apoptosis of cancer cells (Yi et al., 2005\[[@R23]\]). Several compounds such as poncirin, coumarins, auraptine, hesperidin and naringin have been identified from poncirus fruits (Avula et al., 2005\[[@R3]\]). Previously, we reported the chemical compositions of seed essential oil of *Poncirus trifoliata* Rafin by GC-MS and evaluated antibacterial potential of the oil and organic seed extracts of *P. trifoliata* Rafin against foodborne pathogens (Rahman et al., 2009\[[@R16]\]). Further, we have previously reported on the isolation, characterization and anti-listerial potential of naturally occurring limonin and imperatorin from *P. trifoliata* seed (Rahman et al., 2012\[[@R17]\]). However, there is no report available in the literature on antibacterial properties especially on *Xanthomonas* spp. including morphological changes using volatile essential oil, isolated natural compounds of *P. trifoliata*seeds. Considering the deleterious effects of synthetic antibiotics and pesticides on life supporting systems, there is an urgent need to search for alternative approaches for the management of plant pathogenic microorganisms. Therefore, to find out the environmentally friendly alternatives to chemical pesticides we investigated the role of secondary metabolites (essential oil and compounds limonin and imperatorin) of *P. trifoliata*as an antibacterial potential on *Xanthomonas* spp. *in vitro.* Materials and Methods ===================== Micro-organisms --------------- In this study, the used organisms were *Xanthomonas campestris*pv.*compestris* KC94-17-XCC, *Xanthomonas campestris*pv.*vesicatoria* YK93-4-XCV, *Xanthomonas oryzae*pv.*oryzae* KX019-XCO and *Xanthomonas* sp. SK12. These organisms were collected from Korean Agricultural Culture Collection (KACC), Suwon, Republic of Korea. Active cultures for experimental use were prepared by transferring a loopful of cells from stock cultures to flasks and inoculated in Luria-Bertani (LB) broth medium at 28 °C for 24 h. Cultures of each bacterial strain were maintained on LB agar medium at 4 °C. In vitro antibacterial activity assay ------------------------------------- The antibacterial test was carried out by agar disc diffusion method using 100 μl of standardized inoculum suspension containing 10^7^ CFU/ml of bacteria (Murray et al., 1995\[[@R14]\]). The seed essential oil was diluted 1:5 (v/v) with methanol and appropriate amounts (5, 10 or 15 μl) were spotted onto the filter paper discs (6 mm diameter) and placed on the inoculated agar. Negative controls were prepared using the same solvent (MeOH) employed to dissolve the oil. Standard reference antibiotic, streptomycin (20 μg/disc, from Sigma-Aldrich Co., USA), was used as positive control for the tested bacteria. The plates were then sealed with parafilm and incubated at 28 °C for 24 h. Antibacterial activity was evaluated by measuring the diameter of the zones of inhibition against the tested bacteria. Each assay in this experiment was replicated three times. Determination of minimum inhibitory concentration (MIC) ------------------------------------------------------- Minimum inhibitory concentrations (MICs) of seed essential oil and compounds limonin and imperatorin were tested by a two-fold serial dilution method (Chandrasekaran and Venkatesalu, 2004\[[@R7]\]). The test samples of oil and pue compounds (limonin and imperatorin) were dissolved in methanol and dimethyl sulfoxide (DMSO), respectively and incorporated into LB broth medium to obtain a concentration of 1,000 μg/ml and serially diluted to achieve 500, 250, 125, 62.5, 31.25, 15.62, 7.81 and 3.9 μg/ml, respectively. The final concentration of solvent in the culture medium was maintained at 0.5 % (v/v). A 10 μl standardized suspension of each tested organism (10^7^ CFU/ml approximately) was transferred to each tube. The control tubes contained only bacterial suspension, were incubated at 28 °C for 24 h. The lowest concentration of the test samples, which did not show any growth of tested organism after macroscopic evaluation, was determined as MICs, which were expressed in μg/ml. Scanning electron microscopic (SEM) analysis on Xanthomonas spp. ---------------------------------------------------------------- To determine the antibacterial efficacy of the compounds limonin and imperatorin on the morphological changes, SEM studies were performed on *Xanthomonas* sp. SK12 treated with MIC concentrations of these compounds. Controls were prepared without samples. Further, to observe the morphological changes, the method of SEM was modified from Kockro method (Kockro et al., 2000\[[@R12]\]). The bacterial samples were washed gently with 50 mM phosphate buffer solution (pH 7.2), fixed with 2.5 g/100 ml glutaraldehyde and 1 g/100 ml osmic acid solution. The specimen was dehydrated using sequential exposure per ethanol concentrations ranging from 30-100 %. The ethanol was replaced by tertiary butyl alcohol. After dehydration, the specimen was dried with CO~2~. Finally, the specimen was sputter-coated with gold in an ion coater for 2 min, followed by microscopic examinations (S-4300; Hitachi). Statistical analysis -------------------- The data obtained for antibacterial activity of seed essential oil and isolated compounds were statistically analyzed and mean values were calculated. A Student\'s *t*-test was computed for the statistical significance of the results at *p*\< 0.05. Results ======= In vitro antibacterial effect of seed essential oil of P. trifoliata against phytopathogenic Xanthomonas spp. ------------------------------------------------------------------------------------------------------------- Seed essential oil also showed potent *in vitro* inhibitory effect against plant pathogenic bacteria of *Xanthomonas*spp. At the concentrations of 5, 10 and 15 μl/disc of 1:5 (v/v) dilution of seed essential oil with methanol, the oil exhibited a potent inhibitory effect against all four strains of *Xanthomonas*spp. such as *X. campestris* pv. *compestris* KC94-17-XCC, *X. campestris* pv. *vesicatoria* YK93-4-XCV, *X. oryzae* pv. *oryzae* KX019-XCO and *Xanthomonas*sp. SK12 as a diameter of inhibition zones of 13.1\~20.0, 14.0\~22.1, 16.2\~21.0 and 15.2\~21.2 mm, respectively along with their MIC values ranging from 62.5 to 125 μg/ml (Table 1[(Tab. 1)](#T1){ref-type="fig"}). In vitro antibacterial activities of limonin and imperatorin against Xanthomonas spp. ------------------------------------------------------------------------------------- Limonin and imperatorin exhibited potent antibacterial activity against phytopathogenic bacteria of *Xanthomonas*spp. (MIC value: 15.62\~62.5 μg/ml) as shown in Table 2. Bacterium *Xanthomonas*spp. SK12 was found to be the most sensitive organisms toward limonin and imperatorin (MIC: 15.62 μg/ml for each), while *X. campestris* pv. *vesicatoria* YK93-4-XCV was the most sensitive to imperatorin (MIC: 15.62 μg/ml) (Table 2[(Tab. 2)](#T2){ref-type="fig"}). Scanning electron microscopic (SEM) studies on Xanthomonas sp. SK12 using compounds limonin and imperatorin ----------------------------------------------------------------------------------------------------------- On the basis of lower MIC values (15.62 μg/ml) of both limonin and imperatorin on *X.*spp. SK12, the effect of these compounds (MIC) on the morphology of this bacterium was observed by scanning electron microscopy (SEM) and the results showed the detrimental effect of these compounds on the cell morphology of *X.*sp. SK12 (Figure 1[(Fig. 1)](#F1){ref-type="fig"}). Control cells in the absence of limonin and imperatorin showed a regular, smooth surface as shown in Figure 1 (A1-B1)[(Fig. 1)](#F1){ref-type="fig"}. In contrast, cells inoculated with limonin and imperatorin at MIC value (15.62 μg/ml) revealed severe detrimental effect on the morphology of cell membranes, showing disruption, pore formation and analysis of the membranes integrity, as shown in Figure 1 (A2-A3 & B2-B3)[(Fig. 1)](#F1){ref-type="fig"}. Discussion ========== The increasing social and economic implications caused by plant pathogenic bacteria means there is a constant striving to produce safer foods (crops, vegetables and fruits) and to develop new antibacterial agents. In general, plant-derived essential oils are considered as non-phytotoxic compounds and potentially effective against pathogenic bacteria (Vasinauskiene et al., 2006\[[@R22]\]; Basim and Basim, 2003\[[@R4]\]). In recent years, the use of antimicrobial compounds such as essential oils extracts and natural compounds are one of the first choices after outbreaks of bacterial plant diseases. Besides, interest has been generated in the development of safer antibacterial agents to control plant pathogenic bacteria in agriculture which also include essential oils and extracts (Deena and Thoppil, 2000\[[@R8]\]). Essential oils, which are odorous and volatile products of plant secondary metabolism, have wide applications to control pathogenic bacteria (Ozturk and Ercisli, 2007\[[@R15]\]). Various publications have documented the antimicrobial activities of essential oils and plant extracts (Saxena et al., 2012\[[@R20]\]; Shafia et al., 2002\[[@R21]\]; Bougatsos et al., 2004\[[@R5]\]; Jirovetz et al., 2006\[[@R10]\]). Mono- and sesqueterpenes, which are phenolic in nature, have potential antimicrobial activities. It seems reasonable to assume that their antimicrobial mode of action might be related to the phenolic compounds present (Cakir et al., 2004\[[@R6]\]). Most of the studies on the mechanism of phenolic compounds have focused on their effects on cellular membranes. Actually, phenolic compounds not only attack cell walls and cell membranes, thereby affecting their permeability and release of intracellular constituents (e.g. ribose, Na glutamate) but also interfere with membrane functions (electron transport, nutrient uptake, protein, nucleic acid synthesis and enzyme activity). Thus, active phenolic compounds present in the oil of *P. trifoliata* might have several invasive targets which could lead to the inhibition of plant pathogenic bacteria. In our study, it has become clear that seed essential oil strongly inhibited *in vitro* the growth of *Xanthomonas*spp. Bacterial leaf blight caused by *X. oryzae* pv. *oryzae* has been reported the most serious disease of rice in South East Asia, particularly since the widespread cultivation of dwarf high-yielding cultivars (Zhou et al., 2013\[[@R24]\]). Compounds limonin and imperatorin also showed a great potential of antibacterial activity against plant pathogenic bacteria of *Xanthomonas*spp. In this study, *Xanthomonas*sp. SK12 was found to be the most sensitive organism to both limonin and imperatorin. SEM study also revealed the detrimental effect of limonin and imperatorin on the cell morphology of the tested organism such as *Xanthomonas* sp. SK12. The results of this study would be worthy as an important bio-control approach to inhibit such severe plant pathogenic bacteria. Notes ===== Prof. Md. Atiqur Rahman and Prof. Sun Chul Kang (Phone: +82-53-850-6553; FAX: +82-53-850-6559, eMail: sckang\@daegu.ac.kr) contributed equally as corresponding authors. ![*In vitro* antibacterial effect of seed essential oil of *Poncirus trifoliata* Rafin against phytopathogenic*Xanthomonas*spp.](EXCLI-13-1104-t-001){#T1} ![*In vitro* antibacterial effect of limonin and imperatorin on phytopathogenic *Xanthomonas*spp.](EXCLI-13-1104-t-002){#T2} ![Effect of limonin and imperatorin on morphological changes on *Xanthomonas* sp. SK12. Morphological damages of *Xanthomonas* sp. SK12 treated with limonin and imperatorin (MIC 15.62 µg/ml) by scanning electron microscopy (SEM). A1: Control (limonin 0 µg/ml); A2 and A3: Treated with limonin (15.62 µg/ml) showing distorted cell, pore fomation and lysis of cell. B1: Control (imperatorin 0 µg/ml); B2 and B3: Treated with imperatorin (15.62 µg/ml) showing distorted cell, pore fomation and lysis of cell.](EXCLI-13-1104-g-001){#F1}
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1920 United States presidential election in Georgia The 1920 United States presidential election in Georgia took place on November 2, 1920, as part of the wider United States Presidential election. Voters chose 14 representatives, or electors, to the Electoral College, who voted for president and vice president. Background With the exception of a handful of historically Unionist North Georgia counties – chiefly Fannin but also to a lesser extent Pickens, Gilmer and Towns – Georgia since the 1880s had been a 1-party state dominated by the Democratic Party. Disfranchisement of almost all African-Americans and most poor whites had made the Republican Party virtually nonexistent outside of local governments in those few hill counties, and the national Democratic Party served as the guardian of white supremacy against a Republican Party historically associated with memories of Reconstruction. The only competitive elections were Democratic primaries, which state laws restricted to whites on the grounds of the Democratic Party being legally a private club. Vote The Cox/Roosevelt ticket easily carried the state of Georgia on election day. Results References Notes Georgia 1920 Category:1920 Georgia (U.S. state) elections
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To learn more about zebras' mysterious stripes, researchers decided to put black- and white-striped capes over horses. And, aside from feeling more fashionable, the horses attracted less flies, according to researchers from the University of Bristol in the U.K. and University of California Davis. In a study published Wednesday in the peer-reviewed journal PLOS ONE, researchers at a farm in Great Britain detail how flies land on captive zebras and horses dressed in black, white and also black-and-white stripes. Three zebras and nine horses were observed for a total of about 16 hours. Flies appeared just as attracted to naked horses as they were to zebras or horses wearing costumes, but Tim Caro of the University of California notes that flies hardly ever landed on stripes. So, horses wearing black-and-white striped coats appeared to have a sort of insect repellent compared to the animals wearing a solid color. "Stripes may dazzle flies in some way once they are close enough to see them with their low-resolution eyes," Royal Society University Research Fellow Martin How said in a statement. Researchers note this effect was only observed in European flies and flies might not behave the same in Africa. Caro told USA TODAY the next phase of this research will include experimenting with different varieties of stripes and color combinations to try and determine how the stripes "confuse" flies. Follow Ashley May on Twitter: @AshleyMayTweets
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Euclid–Euler theorem The Euclid–Euler theorem is a theorem in mathematics that relates perfect numbers to Mersenne primes. It states that every even perfect number has the form , where is a prime number. The theorem is named after Euclid and Leonhard Euler. It has been conjectured that there are infinitely many Mersenne primes. Although the truth of this conjecture remains unknown, it is equivalent, by the Euclid–Euler theorem, to the conjecture that there are infinitely many even perfect numbers. However, it is also unknown whether there exists even a single odd perfect number. Statement A perfect number is a natural number that equals the sum of its proper divisors, the numbers that are less than it and divide it evenly. For instance, the proper divisors of 6 are 1, 2, and 3, which sum to 6, so 6 is perfect. A Mersenne prime is a prime number of the form ; for a number of this form to be prime, itself must also be prime. The Euclid–Euler theorem states that an even natural number is perfect if and only if it has the form , where is a Mersenne prime. History Euclid proved that is an even perfect number whenever is prime (Euclid, Prop. IX.36). This is the final result on number theory in Euclid's Elements; the later books in the Elements instead concern irrational numbers, solid geometry, and the golden ratio. Euclid expresses the result by stating that if a finite geometric series beginning at 1 with ratio 2 has a prime sum , then this sum multiplied by the last term in the series is perfect. Expressed in these terms, the sum of the finite series is the Mersenne prime and the last term in the series is the power of two . Euclid proves that is perfect by observing that the geometric series with ratio 2 starting at , with the same number of terms, is proportional to the original series; therefore, since the original series sums to , the second series sums to , and both series together add to , two times the supposed perfect number. However, these two series are disjoint from each other and (by the primality of ) exhaust all the divisors of , so has divisors that sum to , showing that it is perfect. Over a millennium after Euclid, Alhazen conjectured that even perfect number is of the form where is prime, but he was not able to prove this result. It was not until the 18th century that Leonhard Euler proved that the formula will yield all the even perfect numbers. Thus, there is a one-to-one relationship between even perfect numbers and Mersenne primes; each Mersenne prime generates one even perfect number, and vice versa. Proof Euler's proof is short and depends on the fact that the sum of divisors function is multiplicative; that is, if and are any two relatively prime integers, then . For this formula to be valid, the sum of divisors of a number must include the number itself, not just the proper divisors. A number is perfect if and only if its sum of divisors is twice its value. One direction of the theorem (the part already proved by Euclid) immediately follows from the multiplicative property: every Mersenne prime gives rise to an even perfect number. When is prime, The divisors of are . The sum of these divisors is a geometric series whose sum is . Next, since is prime, its only divisors are and itself, so the sum of its divisors is . Combining these, Therefore, is perfect. In the other direction, suppose that an even perfect number has been given, and partially factor it as , where is odd. For to be perfect, the sum of its divisors must be twice its value: The odd factor on the right side of (∗) is at least 3, and it must divide , the only odd factor on the left side, so is a proper divisor of . Dividing both sides of (∗) by the common factor and taking into account the known divisors and of gives For this equality to be true, there can be no other divisors. Therefore, must be , and must be a prime of the form . References Category:Theorems in number theory Category:Articles containing proofs Category:Leonhard Euler
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Introduction ============ The Ethiopian mustard \[syn. Abyssinian mustard; *Brassica carinata* *A. Braun*. (2n = 4× = 34); genome B~c~B~c~C~c~C~c~\], is an important leafy vegetable and oilseed crop in northeast Africa ([@B49]). It is evolved as a result of a few interspecific hybridization events between *Brassica nigra* (BB genome, 2n = 2 × = 16) and *Brassica oleracea* (CC genome, 2n = 2× = 18) in Ethiopia. In recent years, this crop is also being utilized for biodiesel production due to its fatty acid composition. In addition, *B. carinata* harbors several genes for resistance to lodging, diseases, and pod shattering; and tolerance to abiotic stresses ([@B15]; [@B46]; [@B30]; [@B12]; [@B50]; [@B44]), which make it also an ideal candidate for broadening the narrow genetic base of canola -- the world's second largest oilseed crop ([@B9]). Dehiscence of fruiting structures is an orchestrated natural mechanism for seed dispersal and survival of many plant species. In Ethiopian mustard and other members of the Brassicaceae family, a dehiscence zone (DZ) is developed between the two valves and the replum, as the pods mature. The highly differentiated cells in DZ weaken the strength of the pods, leading to seed dispersal at maturity. Pod shattering is a highly undesirable trait for commercial seed production in *Brassica* crops and causes significant yield losses of up to 70% in canola ([@B8]). Generally, oilseed Brassicas are 'windrowed' to reduce seed loss due to shattering but this practice is not completely effective ([@B31]). Seed losses accelerate further with the prevalence of high wind velocity and extremely high temperatures during the time of harvesting in Australia. One of the foci of many *Brassica* breeding programs is to develop improved varieties for resistance to pod shattering so the standing crop can be directly harvested with combines without any significant seed loss. Natural variation for shatter resistance exists in the *B. rapa, B. juncea, B. napus*, and *B. carinata* germplasm ([@B22], [@B24]; [@B35]; [@B31]; [@B48]; [@B39]; [@B56]). However, shatter resistance in *B. napus* germplasm is insufficient to reduce yield loss under severe weather conditions ([@B39]). *B. carinata* is reported to be more resistant to seed shattering than *B. napus, B. rapa*, and, *B. juncea* ([@B56]). Interestingly, *B. carinata* is also known to hybridize with the A*~r~* (*B. rapa*) and A~n~C~n~ (*B. napus*) genome species and produce viable 'new type' napus plants (A~n~A~n~C~n/c~C~n/c~) with diverse C~c~ genome ([@B32]; [@B47]; [@B4]; [@B10]). This knowledge prompted us to characterize genetic variation and identify genetic loci for pod shatter resistance in *B. carinata* to improve the level of shattering resistance in other *Brassica* crops, especially in canola. The testing of germplasm for pod shatter resistance under field conditions is often practiced in breeding programs but it is unreliable and confounded with growing environment. However, the availability of test methods like the random impact test and pendulum test to assess the pod strength have made possible the assessment of germplasm to categorize them into shatter tolerant/susceptible under laboratory conditions ([@B22]; [@B29]; [@B18]). The pendulum test relies on the inherent difference in pod strength measured as 'energy used to rupture pods' \[rupture energy (RE)\] ([@B29]). In *B. rapa* and *B. napus*, loci for pod shatter resistance have been delineated using molecular markers ([@B31]; [@B19]; [@B51]; [@B39]; [@B28]). For example, [@B39] reported that several quantitative trait loci (QTL) on chromosomes A03, A09, A10, and C03 account for genetic variation in shatter resistance in the doubled haploid (DH) population derived from BLN2762/Surpass400 as well as in a diverse panel of 181 lines of *B. napus*. Subsequently, [@B28] identified six significant QTL for resistance to pod shatter located on chromosomes A01, A06, A07, A09, C02, and C05 in a diverse panel of 143 *B. napus* accessions, and bi-parental DH and intermated populations derived from the maternal parent, 'R1' (resistant to pod shattering) and the paternal parent, 'R2' (prone to pod shattering). Both these described studies showed that at least one consistent locus on linkage group A09, which maps in the vicinity of *AUXIN RESPONSIVE REGULATOR 18* (*ARR18*) and MADS-box gene, *SHATTERPROOF (BnShp1)*, controls pod shatter resistance in Australian and Chinese germplasm. Several genes which are involved in a complex regulatory network, such as *SHATTERPROOF1 (SHP1)*; *SHATTERPROOF2 (SHP2)*; *FRUITFULL (FUL)*; *INDEHISCENT (IND)*; *ALCALTRAZ (ALC)*; and *REPLUMLESS (RPL)*, control pod shatter resistance in *Arabidopsis thaliana*, and other heterologous systems ([@B14]; [@B38]; [@B42]; [@B26], [@B25]; [@B6]; [@B16]). Some of these genes such as *IND* and *ALC* interact with various hormonal pathways involved in auxin, gibberellins and ABA biosynthesis and regulate pod shattering ([@B45]; [@B3]). To our best knowledge, loci associated for natural variation for pod shatter resistance in *B. carinata* have not been identified yet. This study aims to (i) characterize genetic variation for pod shatter resistance in *B. carinata* accessions, (ii) identify the QTL associated with pod strength in an F~2~ population and a set of 83 accessions, and (iii) determine the physical location of associated QTL on the *B. nigra* (BB genome), *B. juncea* (AB genome), *B. oleracea* (CC genome), and *B. napus* (AC genome) genomes to identify candidate genes underlying shattering resistance in *B. carinata*. Materials and Methods {#s1} ===================== Plant Materials --------------- A diversity panel of 200 accessions of *Brassica* and related species including *B. carinata* (83), *B. rapa* (90), one accession each of *B. barrelieri*, *B. deflexa*, *B. juncea*, *B. maurorum*, *B. oxyrrhina*, *B. ruvo*, *B. tournefortii*, *E. sativa*, *M. longipetala*, *S. alba*, and *S. erysimoides*, two accessions each of *A. thaliana*, *B. nigra*, *B. napus*, and *S. arvensis* and eight accessions of *B. oleracea* were obtained from the Australian Grains Genebank, Horsham ([@B40]). In addition, the F~2~ population comprising 300 individuals was developed from a single F~1~ cross between BC73526 (shatter resistant with high RE) and BC73524 (shattering prone with low RE) to identify the QTL associated with pod shatter resistance. Both parental lines were selected on the basis of their contrasting rupture energy values among 83 accessions of *B. carinata*. Each F~2~ line was selfed to generate F~2:3~ population to confirm phenotypes. Evaluation for Pod Shatter Resistance ------------------------------------- The diversity panel comprising 200 accessions was grown in white plastic pots (10 inch diameter, Garden Plastic city, Australia) in 2012 and 2013 at the Wagga Wagga Agricultural Institute, New South Wales, Australia. Both trials consisted of a 4 range by 100 row array with two replications. Five plants were grown per pot. Passport data on days to first flowering (first open flower on at least two plants in a pot) were recorded. At maturity, five pods from each plant were collected to evaluate for shatter resistance using the pendulum test as described previously ([@B39]). Pod length from each test sample was measured with a scale excluding the length of 'beak' to adjust the position of the pod when pendulum strikes. In the present study, we only focused on 83 *B. carinata* accessions for pod shatter resistance (**Table [1](#T1){ref-type="table"}**). ###### Natural variation for pod shatter resistance in *Brassica carinata* accessions grown under birdcage conditions in 2012 and 2013. Species AGG accession ID Square root predicted means for RE (mJ) Square root SE Backtransformed predicted means for RE (mJ) Square root predicted means for RE (mJ) Square root SE Backtransformed predicted means for RE (mJ) --------------- ------------------ ----------------------------------------- ---------------- --------------------------------------------- ----------------------------------------- ---------------- --------------------------------------------- *B. carinata* ATC90258 1.99 0.18 3.94 1.59 0.19 2.53 *B. carinata* ATC90259 3.29 0.15 10.82 2.50 0.18 6.27 *B. carinata* ATC90260 2.50 0.22 6.26 2.42 0.25 5.84 *B. carinata* ATC90261 3.10 0.19 9.61 2.73 0.18 7.45 *B. carinata* ATC90262 2.63 0.16 6.94 2.83 0.18 8.02 *B. carinata* ATC90263 1.80 0.34 3.22 1.73 0.18 2.99 *B. carinata* ATC90264 2.94 0.20 8.63 2.38 0.23 5.67 *B. carinata* ATC90265 2.96 0.15 8.73 2.45 0.18 6.01 *B. carinata* ATC90266 2.59 0.15 6.73 2.43 0.18 5.91 *B. carinata* ATC93184-1 2.68 0.15 7.18 2.33 0.18 5.44 *B. carinata* ATC93879 3.02 0.16 9.12 1.93 0.18 3.74 *B. carinata* ATC93881 2.29 0.16 5.22 2.72 0.18 7.37 *B. carinata* BC73524 3.16 0.20 9.96 2.18 0.18 4.77 *B. carinata* ATC93884 2.39 0.20 5.73 2.11 0.18 4.43 *B. carinata* ATC93885 2.24 0.16 5.04 2.02 0.18 4.08 *B. carinata* ATC93886 2.16 0.16 4.68 2.76 0.18 7.62 *B. carinata* ATC93887 2.54 0.16 6.47 2.46 0.18 6.04 *B. carinata* ATC93888 2.08 0.26 4.32 1.95 0.18 3.81 *B. carinata* ATC93889 1.53 0.15 2.33 2.68 0.18 7.21 *B. carinata* ATC93890 3.16 0.22 9.98 2.45 0.19 6.00 *B. carinata* ATC93892 2.28 0.15 5.21 2.29 0.18 5.27 *B. carinata* ATC93895 2.88 0.22 8.28 2.14 0.19 4.58 *B. carinata* ATC93896 2.19 0.25 4.78 1.88 0.18 3.55 *B. carinata* ATC93897 2.26 0.34 5.12 \- \- \- *B. carinata* ATC93898 2.63 0.23 6.91 2.69 0.19 7.24 *B. carinata* ATC93899 2.33 0.34 5.44 2.27 0.19 5.14 *B. carinata* ATC93954 3.08 0.24 9.50 2.94 0.25 8.65 *B. carinata* ATC93969 2.70 0.17 7.31 2.76 0.19 7.59 *B. carinata* ATC93971 3.46 0.15 11.96 3.83 0.18 14.67 *B. carinata* ATC93972 3.29 0.21 10.79 3.05 0.19 9.28 *B. carinata* ATC93973 2.06 0.22 4.24 2.09 0.21 4.35 *B. carinata* ATC93974 2.51 0.17 6.28 2.52 0.20 6.35 *B. carinata* ATC93975 3.52 0.18 12.37 3.16 0.18 10.01 *B. carinata* ATC93976 2.69 0.22 7.24 2.68 0.19 7.19 *B. carinata* ATC93977 2.97 0.18 8.80 2.64 0.22 6.95 *B. carinata* ATC93978 3.27 0.27 10.69 3.26 0.20 10.61 *B. carinata* ATC94009 2.39 0.16 5.73 2.32 0.20 5.37 *B. carinata* ATC94010 2.39 0.15 5.72 2.82 0.18 7.96 *B. carinata* ATC94011 2.56 0.15 6.53 1.96 0.18 3.84 *B. carinata* ATC94023 3.15 0.22 9.92 3.09 0.20 9.55 *B. carinata* ATC94024 2.20 0.34 4.85 2.49 0.25 6.19 *B. carinata* ATC94025 \- \- \- 3.04 0.28 9.24 *B. carinata* ATC94035 3.49 0.20 12.17 3.19 0.22 10.15 *B. carinata* ATC94037 2.91 0.22 8.48 2.72 0.25 7.43 *B. carinata* ATC94039 3.23 0.22 10.40 2.63 0.23 6.92 *B. carinata* ATC94041 2.84 0.27 8.09 3.45 0.20 11.90 *B. carinata* ATC94042 3.28 0.26 10.76 1.91 0.18 3.65 *B. carinata* ATC94043 3.27 0.17 10.70 2.90 0.18 8.41 *B. carinata* ATC94044 2.65 0.15 7.00 2.27 0.18 5.15 *B. carinata* ATC94045 3.29 0.18 10.80 3.02 0.18 9.12 *B. carinata* ATC94046 3.10 0.16 9.63 3.69 0.18 13.63 *B. carinata* ATC94047 3.54 0.15 12.50 3.20 0.19 10.26 *B. carinata* ATC94048 2.66 0.16 7.09 2.64 0.18 6.97 *B. carinata* ATC94049 2.98 0.34 8.91 2.53 0.18 6.38 *B. carinata* ATC94050 2.14 0.34 4.58 2.41 0.20 5.80 *B. carinata* ATC94109 2.96 0.19 8.79 3.12 0.21 9.72 *B. carinata* ATC94111 3.06 0.20 9.37 2.01 0.18 4.03 *B. carinata* ATC94113 2.77 0.20 7.70 3.02 0.25 9.14 *B. carinata* ATC94114 3.32 0.21 11.03 2.41 0.28 5.83 *B. carinata* ATC94116 2.41 0.27 5.83 2.56 0.40 6.56 *B. carinata* ATC94117 2.26 0.22 5.12 2.30 0.18 5.31 *B. carinata* ATC94119 2.85 0.17 8.11 2.89 0.19 8.38 *B. carinata* ATC94120 1.76 0.18 3.08 1.96 0.19 3.84 *B. carinata* ATC94125 2.28 0.16 5.21 2.58 0.18 6.66 *B. carinata* ATC94126 4.01 0.17 16.11 4.44 0.20 19.75 *B. carinata* ATC94134 2.67 0.15 7.15 2.15 0.18 4.64 *B. carinata* ATC94135 2.41 0.15 5.82 1.88 0.19 3.55 *B. carinata* ATC94137 2.46 0.17 6.05 1.80 0.18 3.24 *B. carinata* ATC94138 2.06 0.21 4.26 2.51 0.18 6.30 *B. carinata* ATC94139 2.90 0.16 8.43 1.89 0.18 3.56 *B. carinata* ATC94192 1.91 0.24 3.64 2.05 0.19 4.22 *B. carinata* ATC94409 2.08 0.38 4.33 2.70 0.22 7.30 *B. carinata* ATC94411 2.66 0.34 7.08 2.34 0.21 5.47 *B. carinata* ATC94416 2.82 0.26 7.93 2.45 0.22 6.01 *B. carinata* ATC94427 2.15 0.34 4.60 \- \- \- *B. carinata* ATC94429 3.24 0.22 10.51 2.68 0.18 7.17 *B. carinata* ATC94455 2.27 0.18 5.15 2.22 0.18 4.91 *B. carinata* ATC94457 4.50 0.17 20.26 4.56 0.19 20.82 *B. carinata* ATC94458 4.22 0.15 17.83 4.55 0.18 20.74 *B. carinata* ATC94461 2.46 0.18 6.04 2.45 0.20 5.99 *B. carinata* ATC94463 2.39 0.22 5.73 1.89 0.23 3.58 *B. carinata* ATC95065 2.60 0.19 6.74 2.59 0.20 6.70 *B. carinata* ATC95199 2.17 0.15 4.72 2.16 0.18 4.67 *B. napus* BLN2762 1.68 0.16 2.82 1.47 0.18 2.16 Brassica carinata lines were accessed from the Australian Grains Genebank (AGG), Horsham. B. napus accession, BLN2762 was accessed from the Australian National Brassica Germplasm Improvement Program, Wagga Wagga. Pod shatter resistance was tested with pendulum test and expressed as rupture energy (RE) in Millijoule (mJ). RE values were initially square rooted and then back transformed. SE and -, represent to standard error (SE) and missing data, respectively. The two parental lines and their F~2~ population of 300 plants were grown in 2015 in white plastic pots (10 inch diameter, Garden Plastic city, Australia) under birdcage conditions at the Wagga Wagga Agricultural Institute, New South Wales, Australia. Plants were watered daily, fertilized weekly using in-line liquid fertilizers, and protected from aphids. A total of 71 F~2~ plants showed abnormal phenotypes with flower sterility; these individuals were discarded from genetic analysis. Five pods from 229 F~2~ plants (normal phenotype) were collected in the 50 mL tubes containing a silica sachet for further testing of pod rupture energy. Days to flowering was recorded daily for each F~2~ plant. All 229 F~2~ plants were enclosed with pollination bags to get pure F~3~ progenies, while leaving the primary stem out for the natural pod development for shatter testing. Ten F~3~ plants from 229 F~2~ families were grown in 2016 in a 20 row × 12 column array design including nine controls and two parents at Wagga Wagga. Five pods were collected per F~3~ plant. For validation, 58 F~2:3~ families (29 high RE and 29 low RE) and parents were tested with pendulum test as described earlier ([@B39]). Microscopic Analysis of Pod Anatomy ----------------------------------- Anatomical features of pod DZ were observed in 30 random F~2~ plants and five F~2:3~ progenies from 20 F~2~ plants selected on the basis of their rupture energy (10 each with low RE and high RE). Pods were collected at 35--40 days after anthesis. Hand sections were prepared from one cm from the pedicel end of the pod. Fresh sections were observed for autofluorescence using a fluorescence microscope at the Charles Sturt University, Wagga Wagga. Photographs were taken using a Zeiss Axiphot microscope fitted with a Sony Cyber-shot digital camera. Statistical Analyses of Phenotypic Data --------------------------------------- The rupture energy data of an F~2~ population and of a set of 83 diversity lines were square-root transformed to normalize and further analyzed using ASREML in R. Genotype was considered as a fixed effect and environment as random effects. The estimated means for each genotype were used for further genome-wide association analysis. The correlation between rupture energy in 2012 and 2013 was calculated using Pearson's correlation coefficient. RE of five pods of each F~2~ plant was averaged and used for QTL analysis. DNA Isolation and Genotyping ---------------------------- Young leaf tissue of the field grown plants was collected for DNA isolation. Tissue were ground in liquid nitrogen and extracted using a method described in [@B41]. The diversity panel of 83 *B. carinata* accessions and the F~2~ population comprising 300 lines were genotyped with the genotyping-by-sequencing based DArTseq marker approach ([@B39]) at the DArT P/L, University of Canberra, Australia. Genetic Relatedness and Population Structure -------------------------------------------- In order to determine molecular diversity in *B. carinata*, we genotyped 83 accessions with high-quality DArTseq markers having call rate of ≥90%, ≤5% of missing data and minor allele frequency (MAF) of \>0.05. Hierarchical cluster analysis based on Euclidian distance was conducted using the software, PRIMER 6 ([@B7]). Principal coordinate analysis was performed to understand the global diversity among accessions. Bayesian clustering was performed to infer the number of sub-populations among 83 accessions using the software package STRUCTURE v 2.3.4 ([@B37]). The program was run using admixture model with correlated allele frequencies. The presumed sub-population number (*k*) was set from 1 to 5. Ten runs for each *k* were performed with 20,000 burn in period and 50,000 Markov Chain Monte Carlo iterations per run, with no prior information on the origin of individuals. The best *k* value was determined by using the (i) logarithm likelihood for each *k* \[L(*k*)\], (ii) an *ad hoc* quantity (Δ*k*) according to [@B43] and Δ*k* method described by [@B13], respectively. Genotypes were classified into subpopulations based on their membership coefficients estimated in STRUCTURE. Map Construction and QTL Identification for Pod Shatter Resistance ------------------------------------------------------------------ The linkage map of F~2~ population was constructed using DArT P/L's OCD MAPPING program ([@B34]). Markers were clustered into linkage groups according to the method described by [@B52]. Markers with identical genotypes are placed in redundant bins, and the resulting markers/bins within each linkage group were ordered using the traveling salesman path solver program Concorde ([@B2]). The linkage map was constructed for each parent by combining the relevant *in silico* DArT and SNP markers. A linkage map was chosen to be seed map and then a consensus map was constructed using the markers in common for the complete F~2~ population. Two QTL mapping strategies implemented in software packages, GAPIT in the R ([@B27]) and SVS (Golden Helix, Bozeman, MT, United States) were used to identify loci associated with pod shatter tolerance. For GAPIT analysis, we did not correct population structure using principal components in the F~2~ mapping population. Linear marker regression analysis was performed to determine trait-marker associations in the SVS package. The same approach was also followed to reveal the genome-wide association between DArTseq markers and rupture energy among 83 accessions. For GWAS, we selected a set of 54,034 high quality markers which were genotyped across all accessions. To control spurious trait-marker associations, the first 10 eigenvectors (principal components) were calculated in the SVS package. Cryptic relatedness due to ancestry by descent was controlled with the Identity-by-Decent matrix (K matrix). The Mixed Linear Model ([@B36]; [@B55]) adjusted with K-matrix and population structure matrix with PC1 -- PC10 was used to test the trait-marker associations in the SVS package. The *p*-values were adjusted to control the false discovery rate (FDR) of 5%. The significance threshold was determined by applying Bonferroni correction \[*p* = 0.05/6464 (total of markers mapped): 7.73515E~-06~\]. Trait-markers with significance ≤ log(~10~)*p* of 5.11153 were 'declared' as true associations for pod shatter resistance in an F~2~ population. Manhattan plots were generated in the SVS package. Alignment of Markers with the *Brassica* Reference Genomes ---------------------------------------------------------- The physical map positions of significant markers associated with pod shatter resistance were determined using the reference *B. nigra, B. oleracea*, *B. juncea*, and *B. napus* genomes by BlastN ([@B1]) searches, as detailed in [@B39]. The physical positions of pod shatter resistance genes in *A. thaliana* (accessed from TAIR^[1](#fn01){ref-type="fn"}^) were also determined by searching sequence identities with the reference genomes. The top blast significant hits (≥E^-10^) were considered to infer the putative physical positions of markers/candidate genes on the reference genomes, while blast hits to multiple loci with the same top E value were considered to be unmapped onto the reference genome. Results ======= Phenotypic Variation for Pod Shatter Resistance in *B. carinata* Accessions --------------------------------------------------------------------------- There were significant differences (*p* \< 0.001) within the 83 *B. carinata* accessions tested with respect to pod rupture energy that ranged from 1.52 to 4.5 mJ in 2012, and 1.6 and 4.6 mJ in 2013 (**Figures [1A,B](#F1){ref-type="fig"}**). A positive strong correlation (*r* = 0.69) among accessions evaluated across both the 2012 and 2013 growing environments was observed, indicating that RE is genetically controlled (**Figure [1C](#F1){ref-type="fig"}**). Three *B. carinata* accessions, ATC94126, ATC94457, and ATC94458 had 9.14 to 9.63 times higher RE compared to the *B. napus* control genotype, BLN2762 (**Table [1](#T1){ref-type="table"}**). ![**(A)** Natural variation for pod shatter resistance in 83 accessions of *Brassica carinata* evaluated under 2012 and **(B)** 2013 environments, and **(C)** correlation of rupture energy (RE) scores of 83 accessions evaluated under 2012 and 2013 environments. Pod shatter resistance was measured with pendulum test as RE. RE presented for different accessions are square root transformed.](fpls-08-01765-g001){#F1} Genetic Diversity and Population Structure ------------------------------------------ A set of 54,037 high quality DArTseq markers with call rates of \>90% and a reproducibility of \>95% were selected for genetic diversity and population structure analyses to determine whether shatter resistant sources are genetically diverse (**Table [1](#T1){ref-type="table"}**). Hierarchical cluster analysis based on the Euclidean distance revealed five distinct groups at 60% similarity (**Figure [2A](#F2){ref-type="fig"}**). The cluster I was the largest with 75 accessions, followed by three accessions in cluster II (ATC94120, ATC93973, and ATC94192) and cluster IV (ATC90258, ATC94011, and ATC93888). Both cluster III (ATC94409), and cluster V (ATC94109) contained only one accession (**Figure [2A](#F2){ref-type="fig"}**). The overall genetic diversity among accessions was assessed with PCO analysis (**Figure [2B](#F2){ref-type="fig"}**), which revealed similar clustering. There were four clear groups with the majority of the accessions in cluster I. The first three coordinates (PC1 = 15.9%, PC2 = 5.3%, and PC3 = 4.3%) accounted a total of 25.39% of the genetic variation (**Figure [2B](#F2){ref-type="fig"}**), suggesting a weak population structure. The Bayesian -- based clustering analysis using the maximum likelihood distribution LnP(D) of 83 accessions identified two sub-populations as shown in **Figure [2C](#F2){ref-type="fig"}**. The Wilcoxon test also revealed the presence of two subpopulations. Seventy nine accessions were in sub-population I and four accessions were in sub-population II. The STRUCTURE analysis supported the results of cluster analysis; all 83 accessions were grouped in two clusters at 90% similarity (**Figure [2A](#F2){ref-type="fig"}**). ![Molecular diversity among *B. carinata* accessions revealed by 54,034 DArTseq markers. **(A)** Dendrogram of 83 *B. carinata* accessions based on Euclidean distance. A total of 1,000 bootstraps were performed. Clusters with dotted lines were non-significant at the 5% level of significance. Parental lines, BC73526 and BC732524 are markers with inverted triangle (![](fpls-08-01765-i001.jpg)) and square (![](fpls-08-01765-i002.jpg)), respectively. **(B)** A 3D plots of the first three principal coordinates (PCO) of (PCO1, PCO2, and PCO3) showing distribution of the *B. carinata* accessions. The proportion of variation by these axes is given in *parentheses.* **(C)** Population structure of *B carinata* accessions by STURUCTURE. Each accession is represented by a *vertical bar* (labeled as 1 to 83, representing different accessions; detailed in **Table [1](#T1){ref-type="table"}**). Red and light green color bars represent to two subpopulations I and II, respectively. Number of subpopulations were determined on Δ*k* \[the rate of change of LnP(D)\] as shown in **Supplementary Figure [S1](#SM1){ref-type="supplementary-material"}**.](fpls-08-01765-g002){#F2} Genetic Variation and Inheritance for Pod Shatter Resistance ------------------------------------------------------------ Based on the pod shatter resistance (RE) scores, two single plant selections were made from accessions BC73526 (high RE) and BC73524 (low RE) to generate an F~2~ population, representing cluster I (**Figure [2A](#F2){ref-type="fig"}**). Both parental lines of the F~2~ mapping population from the cross, BC73524/BC73526 differed significantly from each other with respect to pod shatter resistance; the shatter prone, maternal parent (BC73524) had the lower RE of 2.2 mJ^(1/2)^ (4.8 mJ) and the resistant, paternal parent (BC73526) had the higher RE of 4.4 mJ^(1/2)^ (19.8 mJ; **Table [1](#T1){ref-type="table"}**). The F~2~ population showed a continuous distribution of RE scores, ranging from 2.2 to 4.7 mJ^(1/2)^ with the mean score of 2.71 mJ^(1/2)^ (**Figure [3](#F3){ref-type="fig"}**). This was typical for quantitative traits such as pod shattering resistance. In order to validate these F~2~ RE scores, we evaluated the F~2:3~ progenies (Supplementary Table [S1](#S3){ref-type="supplementary-material"}). Our results showed that there was a strong positive correlation (*r* = 0.83) between RE scores of F~2~ plants and their F~2~:~3~ progenies, suggesting that phenotypic scores in F~2~ were accurate. ![Frequency distribution of pod shattering scores (rupture energy) in the F~2~ segregation population, containing 229 individuals, derived from BC73526/BC73524. The average RE scores of the parental lines, BC73526 and BC73524 are indicated by solid arrows.](fpls-08-01765-g003){#F3} Multiple Genes Control Pod Shatter Resistance in *B. carinata* -------------------------------------------------------------- A total of 6,464 markers that showed polymorphism between the parents, and segregated in the complete set of F~2~ population (300 lines) were selected for the genetic linkage map construction (Supplementary Table [S1](#S3){ref-type="supplementary-material"}). All of the mapped markers were assigned to the 17 linkage groups, equivalent of haploid genome of *B. carinata*. Of them, 4,981 marker loci were located on the 8 linkage groups of B~c~ subgenome and 1,483 loci were on the 9 linkage groups of C~c~ subgenome, covering a total genetic distance of 1622.82 cM (**Table [2](#T2){ref-type="table"}**). The marker density ranged from 1.07 (C4) to 7.35 (B01) with an average density of 3.98 cM. Chromosome C5 had the least number of markers (78) as compared to B4 (881). This genetic linkage map was further used for the QTL identification. ###### Summary of segregating markers and their coverage on the linkage genetic map of the F~2~ population derived from the BC73524/BC73526 of *B. carinata*. Chromosome Mapped Map length Average ------------------------------ -------- ------------ --------- B1 835 113.61 7.35 B2 634 128.87 4.92 B3 591 117.05 5.05 B4 881 148.70 5.92 B5 667 130.15 5.12 B6 386 90.28 4.28 B7 445 93.27 4.77 B8 542 141.86 3.82 Subtotal of Bc subgenome 4981 963.80 5.17 C1 120 68.19 1.76 C2 113 36.09 3.13 C3 348 109.79 3.17 C4 94 88.12 1.07 C5 78 26.41 2.95 C6 212 71.98 2.95 C7 130 65.11 2.00 C8 120 82.94 1.45 C9 268 110.40 2.43 Subtotal of the Cc subgenome 1483 659.04 2.25 Total of the B~c~C~c~ genome 6464 1622.842 Mean 380.23 95.46 3.98 LG were assigned to eight chromosomes of the B C subgenome and nine chromosomes of the C C subgenome of B. carinata on the basis of their physical map locations on the reference genomes of B. nigra, B. juncea cv\. Tumida (for the B subgenome), B. oleracea (T1000) and B. napus cv\. Darmor (for the C subgenome). We identified five significant QTL (LOD = 3) associated with pod shatter resistance, *Qpsr.wwai-B1a, Qpsr.wwai-B1b*, *Qpsr.wwai-B3*, *Qpsr.wwai-B8*, and *Qpsr.wwai-C5* in the BC73524/BC73526 population (**Table [3](#T3){ref-type="table"}**, **Figure [4A](#F4){ref-type="fig"}** and Supplementary Table [S1](#S3){ref-type="supplementary-material"}). Two QTL; *Qpsr.wwai-B1a* tagged with the *in silico* DArT marker 5863583, and *Qpsr.wwai-B1b* tagged with DArTseq-SNP marker 5858104\|F\| 0-14:A \> T, were located 7.4 cM apart on chromosome B1. Other three QTL, *Qpsr.wwai-B3*, *Qpsr.wwai-B8*, and *Qpsr.wwai-C5* were identified on chromosomes B3, B8, and C5, respectively (**Table [3](#T3){ref-type="table"}**). Of these, *Qpsr.wwai-B1b* accounted for the maximum (5.27%) of the phenotypic variation and the *Qpsr.wwai-C5* accounted for the least (3.71%). All five QTL explained a total of 23.73% of the phenotypic variation for RE. The shatter resistant parent, BC73526 contributed the favorable allele as envisaged by pod strength, and thus reduced pod shattering in progenies. DArTseq markers were assigned the physical positions on *B. carinata* genome, by comparing their sequence identities with the reference genomes of *B. nigra*, *B. juncea, B. oleracea*, and *B. napus*. Our results showed that the *Qpsr.wwai-B1a, qPSR.wwai-B1b*, *Qpsr.wwai-B3*, *Qpsr.wwai-B8*, and *Qpsr.wwai-C5* were located to the pseudomolecules of B1, B3, B8, and C5, respectively (**Supplementary Figure [S2](#SM2){ref-type="supplementary-material"}** and Table [S2](#S4){ref-type="supplementary-material"}). ###### Quantitative trait loci (QTL) associated with pod shatter resistance in the F~2~ population from the BC73526/BC73524. QTL Highly significant marker Chromosomal location Chromosomal position LOD score *R*^2^ (%) *Brassica* reference genome Physical map position (bp) Nearest candidate gene for pod shatter resistance from significant SNP association Physical distance between SNP and candidate gene (kb) ----------------- ---------------------------- ---------------------- ---------------------- ----------- ------------ ----------------------------- ---------------------------- ------------------------------------------------------------------------------------ ------------------------------------------------------- *Qpsr.wwai-B1a* 5863583 B1 49.8 9.86E-05 5.09 *B. nigra*/CM004491.1"\_B1 19,563,260 *FUL* 63.12 *Qpsr.wwai-B1b* \#5858104\|F\| 0-14:A \> T B1 57.2 7.45E-05 5.27 CM007195.1"\_B1 Unknown *FUL* 8263.23 *Qpsr.wwai-B3* 4119205\|F\|0-39:G \> A B3 58.5 0.0002 4.65 *B. nigra* CM0044931.1"\_B3 32,518,934 *IND* 2493.1 *Qpsr.wwai-B8* 5847615 B8 77.0 0.0001 5.01 *B. nigra*/CM004498.1"\_B8 31,742,473 *RPL* 1131.55 *Qpsr.wwai-C5* 3107471 C5 16.2 0.000832 3.71 *B. oleracea*"\_/C~n~5 11,396,951 *FUL* 454.62 Reference genomes of B. nigra , B. juncea cv\. tumida, version 1.0, B. oleracea (T1000) and B. napus version 4.1, were used for sequence alignments against B. carinata sequences. Details of alignments with the pseudomolecules of B. juncea and B. napus are given in the Supplementary Table S2 . \#Appropriate physical location based on the bin markers. ![Manhattan plots showing **(A)** marker- pod shatter resistance associations and **(B)** marker-pod length associations, in the F~2~ population from BC73524/BC73526 using GAPIT analysis. Highly significant markers are also shown; marker depicted with \>denotes DArTseq SNP markers and without \>symbol denotes *in silico* DArT. The suggestive threshold LOD value (3.0) for trait-marker association is shown as dashed line.](fpls-08-01765-g004){#F4} To establish whether pod length relates to pod shattering, we mapped QTL associated with pod length in the F~2~ population. Our results showed that one significant marker, 5859132\|F\| 0--7:T \> G at QTL (LOD = 3.55) was associated with pod length in the F~2~ population (**Figures [3](#F3){ref-type="fig"}**, **[4B](#F4){ref-type="fig"}**, and Supplementary Tables [S2](#S4){ref-type="supplementary-material"}, [S3](#S5){ref-type="supplementary-material"}). This QTL was identified on chromosome B8 and mapped 1 cM apart from the pod shatter resistance QTL, *Qpsr.wwai-B8*. Two other markers, 5832583 and 5863583 on chromosome B1 also showed association with pod length (LOD scores of 2.7 to 2.9, Supplementary Table [S3](#S5){ref-type="supplementary-material"}). GWAS analysis using 54,034 markers based polymorphisms was performed to verify the alleles for pod shatter resistance in diverse *B. carinata* accessions Although, we used a small number of accessions for this analysis, we found 19 statistically significant SNP associations between markers and pod shatter resistance (RE scores) based on the Bonferroni corrected threshold --log 10(*p*) = 9.25292E^-07^ (Supplementary Table [S3](#S5){ref-type="supplementary-material"}). By controlling type 1 error using kinship coefficients (IBS) and first 10 principal components at least 16 consistent significant associations were identified across both 2012 and 2013 trials with LOD score of ≤5.35 (Supplementary Tables [S3](#S5){ref-type="supplementary-material"}, [S4](#S6){ref-type="supplementary-material"}). Physical Mapping of Significant QTL and Alignment with *Brassica* Reference Genomes ----------------------------------------------------------------------------------- Of 6464 DArTseq markers mapped, the chromosomal positions of 5,080 markers could be linked with the pseudomolecule positions to the published genome sequences of *B. oleracea*, *B. napus, B. juncea*, and *B. nigra* (Supplementary Table [S1](#S3){ref-type="supplementary-material"}). We also anchored several scaffolds which have been unmapped yet to the pseudomolecules of *B. juncea* genome assembly in an F~2~ population. Furthermore, marker sequences targeting QTL were aligned with the sequenced reference B, C and AC genomes and physical intervals harboring candidate genes for pod shatter resistance. Of the seven pod shatter resistance genes of *A. thaliana* searched, *FUL --* a MADS box gene negatively regulated by *APETALA1* (TAIR ID: AT5G60910.1), was located 63.1 kb away from the significant SNP marker, 5863583 on chromosome 1B (**Table [3](#T3){ref-type="table"}**). Other candidate genes were located 0.4 to 8.3-Mbp apart from corresponding QTL regions in the F~2~ population (Supplementary Tables [S4](#S6){ref-type="supplementary-material"}, [S5](#S7){ref-type="supplementary-material"}). We identified 40 GWAS SNP associations (LOD ≤ 3) in the proximity (5.1 kb to 16 Mbp) of genes controlling pod shattering in *A. thaliana*. Of them, three orthologs of *FUL* were located on chromosome B1 (5.1 kb), B6 (97.4 kb) and on the LFLV01001230.1scaffold_28.1 of the reference genome of *B. nigra* (34.69 kb), while two orthologs of *IND* were located on chromosome B1 (53.69 kb) and B2 (96.77 kb). One ortholog of *SHP2* was also identified within 77 kb region of chromosome B5 corresponding to SNP association with 100067358\|F\| 0-31:T \> C marker (Supplementary Table [S5](#S7){ref-type="supplementary-material"}). Pod Shatter Resistance Is Related with Pod Dehiscence Zone Differentiation in *B. carinata* ------------------------------------------------------------------------------------------- Pod structure was observed (40 days after anthesis) under a fluorescence microscope to determine any link between the pod DZ differentiations and shatter resistance in *B. carinata*. The anatomical feature of parents displayed a distinctive difference in the valve margin formation (**Figure [5](#F5){ref-type="fig"}**). The shatter prone parent, BC73524 had the well-developed DZ comprising thin walled parenchymatous cells (**Figure [5a](#F5){ref-type="fig"}**) compared to the shatter resistant parent, BC73526 (**Figure [5b](#F5){ref-type="fig"}**). Thirty randomly selected F~2~ plants exhibited a varied level of DZ development pattern (**Figures [5d](#F5){ref-type="fig"}--[i](#F5){ref-type="fig"}**). For example, there was either clear DZ along the whole valve margin (**Figure [5e](#F5){ref-type="fig"}**), similar to shatter prone parent (**Figure [5a](#F5){ref-type="fig"}**); loss of DZ proximal to the main vascular bundle (mv) as well as near the outer part of the replum (**Figure [5d](#F5){ref-type="fig"}**), similar to the shatter tolerant parent (**Figure [5c](#F5){ref-type="fig"}**); and DZ proximal to the main vascular bundle (mv) but did not extend near the outer part of the replum (**Figure [5h](#F5){ref-type="fig"}**). In *B. napus*, a well-developed DZ was clearly evident (**Figure [5c](#F5){ref-type="fig"}**) similar to the shatter prone *B. carinata* parent, BC73524. ![Anatomical features of dehiscence zone also called abscission layer in parents and F~2~ plants of the BC73524/BC73526. **(a)** BC73524, **(b)** BC73526, **(c)** *B. napus* advanced breeding line, BLN2762 and **(d--i)** F~2~ plants with varying level of dehiscence zone development. Transverse pod section of BC73524 showing well-developed DZ whereas BC73526 showing almost no DZ differentiation. V: valve, VB: vascular bundle of ruplum, en: endocarp, ep: epicarp, me: mesocarp.](fpls-08-01765-g005){#F5} Discussion ========== Considering the commercial value of oilseed *Brassica* crops (*B. napus*, *B. rapa*, and *B. juncea*) worldwide, genetic improvement for pod shatter resistance is of paramount importance to reduce unwanted losses. Despite of limited genetic diversity in *B. carinata* germplasm ([@B21]; [@B17]), several accessions were found to be useful in uncovering genetic variation for resistance to pod shatter (**Table [1](#T1){ref-type="table"}**). For example, we found three accessions which had more than nine times higher pod RE as compared to the *B. napus* control genotype, BLN2762. Genetic variation in these accessions could be harnessed for further genetic improvement of *B. carinata* as well as other *Brassica* species. We determined the pod strength (RE) in *B. carinata* with pendulum test, as a proxy for shatter resistance. This method was found to be reliable and repeatable in determining the extent of pod-shatter resistance and mapping QTL in *B. carinata* (this study, **Table [3](#T3){ref-type="table"}** and Supplementary Table [S4](#S6){ref-type="supplementary-material"}). Similar findings were made in previous studies on genetic variation for pod shatter resistance in *B. rapa* and *B. napus* ([@B22], [@B24]; [@B35]; [@B31]; [@B48]; [@B39]; [@B56]). We revealed that pod shatter resistance is due to multiple genes in the F~2~ population of *B. carinata* derived from the BC73524/BC73526. Multigenic inheritance for pod shatter resistance in *B. carinata* (this study) is consistent with previous findings in *B. rapa* and *B. napus* ([@B31]; [@B51]; [@B39]; [@B28]). In this study, a linkage map of a F~2~ population was constructed utilizing 6,464 DArTseq markers and subsequently used for QTL analysis. The marker density of this linkage map (**Table [2](#T2){ref-type="table"}**) was comparable with the linkage map of a DH population of *B. carinata* derived from YW ([@B57]). The majority of DArTseq markers were linked with the physical positions on the reference genomes of *B. nigra/B. juncea* and *B. oleracea*/*B. napus*. In addition, several scaffolds which were unassembled in the reference *B. juncea* sequence ([@B54]) could be mapped to the linkage map of *B. carinata* population (Supplementary Table [S1](#S3){ref-type="supplementary-material"}). Our results suggested that the reference genomes are useful in anchoring different linkage groups to pseudomolecules and facilitating molecular marker and candidate gene discovery. One of the QTL, *Qpsr.wwai-B1a* delimited with marker 5834957 was mapped to the B1 pseudomolecule of *B. nigra* within 63.12 kb of Arabidopsis *FUL* ortholog (Supplementary Table [S4](#S6){ref-type="supplementary-material"}). [@B33] showed that ectopic expression of the Arabidopsis *FUL* gene in *B. juncea* is sufficient to produce pod shatter resistance, via negative regulation of the valve-margin identity genes ([@B14]). However, the transgenic *B. juncea* fruit produced were too tightly closed. Similar observations were made in this study, the shatter resistant accession BC73526 did not dehisce under natural field conditions and there was no clear separation between valve margin and replum (**Figure [5](#F5){ref-type="fig"}**). A close link between pod shatter resistance and DZ differentiation was observed, the shatter prone and shatter tolerant accessions could be differentiated based on pod anatomy. The shatter prone accession (BC73524) had a well-developed DZ as compared with shatter resistant (BC73526). Similar observations have been made in *A. thaliana*, *B. rapa*, *B. napus*, and *B. carinata* ([@B23]; [@B20]; [@B14]; [@B45]; [@B39]). Several genes; *FUL*, *SHP1*, *SHP2*, *ALC*, *IND*, and *RPL* have been implicated in the development of the valve-margin separation layer, and lignification of the endocarp layer ([@B11]). [@B16] showed that homozygous *braA.ind.a* mutants showed a clear loss of valve margin formation in *B. rapa* and *B. oleracea.* The marker 5834957 at *Qpsr.wwai-B1a* also showed the complete linkage with other loci; 5861424, 5832583, 5843024, 5854441, 5842255, 5843155, and 5849931. These markers were mapped at the 49.81 cM of the F~2~ map and showed significant sequence identities with the A09 reference genome sequence of *B. juncea* (coordinates 6,440,430 to 7,118,167 CM007193.1_chromosome_A9, coordinate 6480570bp, 1.84E-25) (Supplementary Table [S1](#S3){ref-type="supplementary-material"}). In previous studies, a major QTL for pod shatter resistance was located on chromosomes A09/C08, in the vicinity of *SHATTERPROOF* gene in *B. napus* populations ([@B19]; [@B39]; [@B28]). We searched the *SHP1* and *SHP2* orthologs in the reference genome of *B. juncea*. One of the *SHP1* homologs was mapped ∼35 Mb away from the highly significant SNP marker 5834957 on pseudomolecule A09 of *B. juncea* \[sequence identity = 323 bits (163), Expect = 3e-86, 211/227 (92%); coordinates 45,984,225 to 45983999 (Supplementary Table [S4](#S6){ref-type="supplementary-material"})\]. While, one of the six *SHP2a* (JQ973082.1 *B. napus SHATTERPROOF* mRNA) homologs was located in the vicinity of the highly significant SNP marker 5834957 on chromosome B1/A09 \[313 bits, score: 2e-83, Identities = 176/182 (96%)\]. In addition to *SHP2* and *FUL*, other genes controlling pod shatter resistance such as *IND* were also mapped near the statistical significant marker associations (**Table [3](#T3){ref-type="table"}**), suggesting the markers identified for pod shatter resistance herein are reliable. Conclusion ========== We mapped QTL controlling pod shatter resistance in *B. carinata* and identified sequence-based molecular markers. These trait-marker associations with respect to reference genomes of *B. napus*, and *B. juncea* could also pave the way for delineation of pod shatter resistance QTL involved in natural variation, map-based cloning of those QTL and unravel the molecular architecture of pod shatter resistance genes in natural germplasm of *B. carinata*. In addition, molecular markers identified herein will enable us to trace the introgression of pod shatter resistance alleles for strategic improvement of *B. carinata*, *B. napus*, and other related species. Previous studies have reported that there is limited genetic variation for pod shatter resistance in the natural *B. napus* germplasm ([@B5]; [@B39]). Several research groups around the world are currently using *B. carinata* to expand the narrow genetic base of *B. napus* germplasm ([@B9]; [@B10]). In this study, only one QTL, *Qpsr.wwai-C5* was identified on the C subgenome of *B. carinata* (chromosome C05), while other QTL were identified on the B subgenome (B1, B3, and B8). Previous studies have shown that fertile plants of *B. napus* carrying B genome introgressions can be generated ([@B32]; [@B10]). It remains to be established whether B and C genome derived lines exhibit pod shatter resistance expression or get silenced in the resynthesized *B. napus* ([@B53]). Nevertheless, our results provide valuable information on donor sources for pod shatter resistance, genetic inheritance, genetic map location of QTL, and associated markers for marker-assisted selection. The markers identified in this study can be assayed on any sequencing platform and/or converted into simple KASP assay for high throughput analysis. Author Contributions ==================== RR and HR designed the study, and prepared the manuscript. RR developed F~2~ and F~3~ populations, conducted the experiments and analyzed the data. NC designed the field trials and RR and NC analyzed the data, YQ assisted in phenotyping, performed pod anatomy, and DNA extractions. AK and JS aligned DArTseq data with the reference genomes. All authors reviewed and edited the manuscript. Conflict of Interest Statement ============================== AK is the director of Diversity Arrays Technology Pty Ltd. and JS was employed by Diversity Arrays Technology Pty Ltd. All other authors declare no competing interests. **Funding.** We thank the Grains Research and Development Corporation and NSW DPI for the investment made to support this research under the project, DAN00208. Authors thank Dr. Bob Redden, Australian Grains Genebank, Horsham, Australia for providing the *B. carinata* accessions, Ms. Louisa Slinger and Mr. John Bromfield for pendulum testing. <https://www.arabidopsis.org> Supplementary Material ====================== The Supplementary Material for this article can be found online at: <https://www.frontiersin.org/articles/10.3389/fpls.2017.01765/full#supplementary-material> ###### Click here for additional data file. **FIGURE S1 \|** Analysis of the population structure of 83 *B. carinata* accessions. The likelihood values \[Ln(P(D\] for each successive K. ###### Click here for additional data file. ###### Click here for additional data file. **FIGURE S2 \|** Manhattan plots showing marker-pod shatter resistance associations in the F~2~ population using the SVS package. A linear markers regression analysis was performed to identify loci associated with pod rupture energy. ###### Click here for additional data file. ###### Click here for additional data file. ###### Click here for additional data file. ###### Click here for additional data file. ###### Click here for additional data file. ###### Click here for additional data file. [^1]: Edited by: *Maoteng Li, Huazhong University of Science and Technology, China* [^2]: Reviewed by: *Yan Long, Chinese Academy of Agricultural Sciences, China; Liezhao Liu, Southwest University, China* [^3]: This article was submitted to Crop Science and Horticulture, a section of the journal Frontiers in Plant Science
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Q: How many 10 letter 'words' can be made with no repeated letters and at least 8 consonants? Need a little bit of help with this one. How many 10 letter 'words' can be constructed which have no repeated letters and at least 8 consonants? where 'word' is defined as any combination of the 26 letters of the english alphabet, and by consonant, (obviously) a letter of the english alphabet that are not either a,i,u,e, or o. This is where I am at: We need to choose the positions for the 8 consonants which is $c(10,8)$ Then we need to choose the 8 consonants which I think is $p(21,8)$? (not sure about this one) Choose the remaining 2 letters: We have already used 8 letters so we only have 18 letters to choose from so $p(18, 2)$ What else needs to be calculated? Do we need to choose the position of the remaining 2 letters? A: I think the best way would be to separate it into 3 non-overlapped groups: Words with exactly 8 consonants Words with exactly 9 consonants Words with exactly 10 consonants Logic would be similar with Arturo. Arvin comments wouldn't work, because you count same words several time. Once when the consonant is one of the 8, and again, when it happens to be one of the two remaining letters. For the 8 consonants: Select 8 positions - C(10,8) Select the 8 consonants out of the 21, in order - P(21,8) Select the 2 vowels in order - P(5,2) So answer is: c(10,8) * p(21,8) * p(5,2) = (10!/(2!*8!)) * (21!/13!) * (5!/3!) = 45 * (21!/13!) * 20 Similarly, do the same for 9 and 10: 9 consonants: C(10,9) * P(21,9) * P(5,1) = 10 * (21!/12!) * 5 = 50 * (21!/12!) 10 consonants: C(10,10) * P(21,10) * P(5,0) = (21!/11!) Sum the 3 answers. A: Your argument has a couple of problems: You don't specify where the last two letters selected go; you pick the two letters, but you never place them; placing them in different order gives you different solution. Likewise, you never say how you will distribute the 8 consonants you pick; you select the 8 locations, but you don't say which letter goes where. Finally, your solution counts some words too many times. Say you first select the eight consonants b,c,d,f,g,h,j,k and the first eight positions for them (in that order). Then you select two more letters, say m,n, and place them in order in positions nine and ten. You will "count" this word again if your eight selected consonants are b,c,d,f,g,h,m,n, the eight positions selected are positions one through six, nine, and ten (in that order); and then the other two letters you select are j and k and you place them in positions seven and eight. You will count this word several times through your process. So: perhaps it's better if we start by counting how many 10 letter strings have exactly eight consonants and no repeated letters. My recommendation: First select the eight positions that will contain the consonants. Then select the consonants and place them in those positions in order (that is, which consonant you select first matters, because that will go in the leftmost selected position). Finally, select the two vowels that will fill the remaining two positions, again in order. Then count how many of your strings have exactly 9 consonants in a similar manner; then how many have all letters consonants (that will be the simplest one).
3.03125
3
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Hope for halting incurable citrus disease Sep. 25, 2013 — The devastating disease Huonglongbing, or citrus greening, looms darkly over the United States, threatening to wipe out the nation's citrus industry, whose fresh fruit alone was valued at more than $3.4 billion in 2012. Recently, however, a research team led by a University of California, Davis, plant scientist used DNA sequencing technologies to paint a broad picture of how citrus greening impacts trees before they even show signs of infection, offering hope for developing diagnostic tests and treatments for the currently incurable disease. "Florida is seemingly in the death grip of citrus greening, and many experts believe it is just a matter of time before the disease appears full force in California," said plantmolecularbiologist Abhaya Dandekar, lead author on the study. The new findings indicate that the bacterial disease interferes with starch and sugarmetabolism in young and matures leaves and fruit, while also wreaking havoc with hormonal networks that are key to the trees' ability to fend of infections. Study results will be reported Sept. 25 in the journal PLOS ONE. "Because the disease has a long latent phase during which there are no symptoms of infection and the bacteria are resistant to being grown in the laboratory, the only option for halting transmission of citrus greening has been to apply chemicalpesticides to control the insect that spreads the bacteria," Dandekar said. About citrus greening: HLB, or citrus greening, is the most destructive citrus disease worldwide. It is caused by three species of the Candidatus Liberibacterbacteria, including Candidatus Liberibacter asiaticus, which is known by the acronym CaLas. These bacteria are carried from tree to tree by two species of the citrus psyllid, a winged insect that is about one-eighth inch long and attaches itself to the underside of the trees' leaves. As the citrus psyllid feeds on a leaf, it can pick up the bacteria from a diseased tree and introduce the bacteria to a non-infected tree. These disease-causing bacteria reside in the tree's phloem -- the vascular tissue that carries vital nutrients throughout the tree. The disease affects most citrus species, causing yellowing of shoots, blotchy and mottled leaves, lopsided and poorly colored fruit and loss of viable seeds. The fruit of diseased trees is hard, misshapen and bitter, and the infected trees die within a few years. Other than one infected backyard tree found in 2012 in the Southern California community of Hacienda Heights, the disease has not been detected in California. However the citrus psyllid that transmits the bacteria was first found in California in 2008 and has since been identified in San Diego, Imperial, Riverside, San Bernardino, Orange, Los Angeles, Ventura, Santa Barbara, Kern and Tulare counties, resulting in quarantines and restricted areas. The new study: In this new study, the researchers studied four categories of healthy and diseased citrus trees, with the goal of better understanding how HLB affects trees physiologically during the very early stages of infection. "Earlier sequencing of the CaLas bacteria genome showed that there were no toxins or enzymes that would destroy plantcell walls, or specialized secretion systems associated with citrus HLB," Dandekar said. "Because these factors, which normally accompany plant diseases, were not present, we suspected that the disease was causing metabolic imbalances or interfering with nutrient transport in the infected trees," he said. The researchers used gene sequencing technology to study the "transcriptome," which is the collection of RNA found in the tree leaves and fruit. Furthermore, the researchers discovered that HLB interfered with the regulation of hormones such as salicylic acid, jasmonic acid and ethylene, which are "the backbone" of the plant innate immune response. And they found that infected trees also had changes in the metabolism of important amino acids that serve as a reservoir for organicnitrogen in many plants. The nitrogen is required to stimulate the plant immune response. Cause for hope: The researchers anticipate that these discoveries will lead the way to new tests for detecting the bacteria and thus the presence of HLB in orchard trees. They also suggest that it may be possible to develop several short-term treatments for infected trees. Such therapeutic procedures might rely on using hormones and other small molecules to restore the infected tree's normal metabolism or boosting the tree's innate immune response to effectively fight the infection. Feedback Tell us what you think of Chemistry 2011 -- we welcome both positive and negative comments. Have any problems using the site? Questions? Your Name:Your Email:Comments:Click button to submit feedback: About us Chemistry2011 is an informational resource for students, educators and the self-taught in the field of chemistry. We offer resources such as course materials, chemistry department listings, activities, events, projects and more along with current news releases. The history of the domain extends back to 2008 when it was selected to be used as the host domain for the International Year of Chemistry 2011 as designated by UNESCO and as an initiative of IUPAC that celebrated the achievements of chemistry. You can learn more about IYC2011 by clicking here. With IYC 2011 now over, the domain is currently under redevelopment by The Equipment Leasing Company Ltd. Events & Activities Are you interested in listing an event or sharing an activity or idea? Perhaps you are coordinating an event and are in need of additional resources? Within our site you will find a variety of activities and projects your peers have previously submitted or which have been freely shared through creative commons licenses. Here are some highlights: Featured Idea 1, Featured Idea 2. About you Ready to get involved? The first step is to sign up by following the link: Join Here. Also don’t forget to fill out your profile including any professional designations.
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Q: Prolog Assigning integer to a variable I'm new to Prolog, and using GNU Prolog, so no clp(fd) allowed. What I'm trying to do is for a given integer N, generate a list with elements of 1 ~ N. So set(3,T). will output T = [1,2,3]. Here is what I have so far: set(0,[]). set(N,T):-set(N-1,T1),append(T1,[N],T). When I try set(2,T), it crashes. I debugged with trace, and find out that it's not evaluating N-1, but rather doing N-1-1-1... Anyone can tell me how to solve this? Thank you. A: It should be: set(N,T):- N2 is N-1, set(N2,T1), append(T1,[N],T). Arithmetic operations are performed by using is/2. N-1 is a shorthand for -(N,1) (just like N2 is N-1 is shorthand for is(N2, N-1)), so you were just creating infinite tree -(-(-(-(...),1),1,1,1). Little educational note: If you want set/2 to be proper relation so it can answer queries like set(3,X), set(X, [1,2,3]) and set(X,Y) without error then you should write this predicate that way: set(0, []). set(Value, List) :- length(List, Value), append(ShorterList, [Value], List), ValueMinusOne is Value - 1, set(ValueMinusOne, ShorterList). That way result of arithmetic operation is always possible to obtain because input value (lenght of the list) is either explicitly given or generated from length/1.
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Aug 22, 2016· A36 steel is a structural billet steel for structural applications. A36 is a material grade and designation defined in ASTM A36/A36M08 standard. ASTM A36/A36M08 is an international material standard for billet steel for general structural usage.What is the international equivalent grade for steel Sep 07, 2015What is an ASTM A36 Steel equivalent? See more results A36 steel is a common structural steel in the United States. The A36 standard was established by the ASTM InternationalProperties· A36 vs. 1018 Steel Comparison | Capital Steel & Wire A36 vs. 1018 Steel Comparison. As two of the most highly sought after steel grades on the market, many questions come up between the differences in 1018 and A36 steel. How different is A36 from 1018? Are they equivalent material grades? We thought it would be best to provide a comparrison for A36 and 1018 steel. leecosteel› Steel Plate ProductsASTM A36 steel plate is one of the most widely used carbon structural steels used in the industry. It can be riveted, bolted or welded in the construction of bridges and buildings, and for general structural purposes. ASTM A36 is known to be an equivalent to EN S275 steel plate. A36 vs. 1018 Steel Comparison. As two of the most highly sought after steel grades on the market, many questions come up between the differences in 1018 and A36 steel. How different is A36 from 1018? Are they equivalent material grades? We thought it would be best to provide a comparrison for A36 and 1018 steel. What Is A36 Steel? | Hunker A36 Steel is the American Society for Testing and Materials (ASTM) designation for carbon steel. ASTM A36 steel is the most common type of steel used in construction. Its properties allow the steel to be used in many applications, unlike higherperformance alloys. leecosteel› Steel Plate ProductsASTM A36 steel plate is one of the most widely used carbon structural steels used in the industry. It can be riveted, bolted or welded in the construction of bridges and buildings, and for general structural purposes. ASTM A36 is known to be an equivalent to EN S275 steel plate. ASTM A36 Mild/Low Carbon Steel AZoM ASTM A36 is the most commonly used mild and hotrolled steel. It has excellent welding properties and is suitable for grinding, punching, tapping, drilling and machining processes. ASTM A36 Mild/Low Carbon Steel. Download PDF Copy; Written by AZoM Jul 5 2012. Topics Covered. Introduction Can we say that A 36 is carbon steel since it has Steel Plate Grades. Width Length; 3/16″ – 8″ 36″ to 120″ Commercial and Specification Grade Steel Plates are stocked to meet a variety of end use requirements that range from the most unsophisticated storage bin to such highly critical applications as Cryogenic Pressure Vessels. ABS Steels Wikipedia ABS Steels are types of structural steel which are standardized by the American Bureau of Shipping for use in shipbuilding. The 36 grades have yield strength of 51,000 psi (355 MPa), and ultimate tensile strength of 71,000 90,000 psi (490620 MPa).Basic properties· Steel plate is processed by flame cutting or High Def Plasma cutting. Hi Def Plasma is utilized to sizes 1" and under, over 1" is flame cut. A36 Steel plate has a 36,000 min yield strength. Steel Plate. Steel plate A36 is stocked in all pattern sizes up to 96" x 288" and can be processed to special shapes per print. ASTM A131 Steel, Grade AH36 MatWeb UNS K01806, Structural steel used in ship construction Highstrength, lowalloy Materials as large as 13mm thick may be semikilled Product Description: shipbuilding steel stock ABS,LR shipbuilding steel steel for shipbuilding and oil platform: Henan BEBON Iron & Steel Co., Ltd , is professional in exporting the steel for shipbuilding and oil platform. Our product have the following several feature 1.The size of steel plates we can supply is 3mm-180mm * 1250mm-4000mm * 3000mm-18000mm 2.The main standard our steel is according to ASTM A131,API. 3.The main classification society we cooperate are: ABS ,GL, LR, BV, NK,DNV,KR,RINA. 4.Productive technology: HR,CR,TMCP,N,Q&T,IMPACT TEST,Z15,Z25,Z35. 5.Hard stamp about the brand of manufacturer, Heat No.,Batch No., steel grade, steel size, and the brand of Classification Society. 6.Blasting according to SA2.5 standard, and the shop primed on the steel, coating thickness is 15-35 micrometer.
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Multiple access schemes are employed by modern radio systems to allow multiple users to share a limited amount of bandwidth, while maintaining acceptable system performance. Common multiple access schemes include Frequency Division Multiple Access (FDMA), Time Division Multiple Access (TDMA) and Code Division Multiple Access (CDMA). System performance is also aided by error control codes. Nearly all communications systems rely on some form of error control for managing errors that may occur due to noise and other factors during transmission of information through a communication channel. These communications systems can include satellite systems, fiber-optic systems, cellular systems, and radio and television broadcasting systems. Efficient error control schemes implemented at the transmitting end of these communications systems have the capacity to enable the transmission of data including audio, video, text, etc., with very low error rates within a given signal-to-noise ratio (SNR) environment. Powerful error control schemes also enable a communication system to achieve target error performance rates in environments with very low SNR, such as in satellite and other wireless systems where noise is prevalent and high levels of transmission power are costly, if even feasible. Interleave Division Multiple Access (IDMA) is a multiple access technique where different users that share the same bandwidth and time slots are separated by user specific interleavers. As the bandwidth and power become scarce to support the ever increasing throughput requirements, more complex but more efficient techniques play more important roles in future communication systems. IDMA is an effective technique that trades extra receiver complexity with bandwidth and power savings. On the other hand, in systems where the number of users is high and the block size is large, storage of a high number of long interleavers may be undesirable. Scrambled Coded Multiple Access (SCMA) addresses this complexity by using a single scrambling sequence with different shift factors for different users without any performance penalty. With SCMA, the user specific interleavers of IDMA are replaced with user specific scrambler sequences. While there is no noticeable performance difference between the two approaches, generation and implementation of scrambler sequences is significantly simpler. In fact, the same scrambler sequence with different rotation factors can be used for different users with no impact on performance, which further reduces receiver complexity. With SCMA, therefore, all of the benefits of IDMA are achieved with reduced complexity. Similar to IDMA or random waveform Code Division Multiple Access (CDMA), SCMA is a non-orthogonal multiple access technique. While orthogonal multiple access schemes such as Time Division Multiple Access (TDMA) or Frequency Division Multiple Access (FDMA) are implicitly too restrictive to achieve theoretical limits in fading channels, non-orthogonal CDMA, IDMA or SCMA have the potential of achieving these limits. Further, as discussed above FEC coding is typically used to improve the performance. The main difference between CDMA and SCMA is that, while in CDMA different users are separated with different signature sequences with a spreading factor greater than one, in SCMA even a spreading factor of one would be enough to detect overlapped users based on user specific scrambler sequences and iterative multiuser cancellation with FEC decoding. As a result, the available bandwidth can be used for very low rate coding which gives SCMA extra coding gain that is not available in CDMA. Actually it is also possible to use SCMA with a spreading factor greater than one. Another benefit of the iterative receiver structure of SCMA is that the system performance actually improves with power variations among the users, which eliminates the need of power control, an important requirement of traditional CDMA. At the receiver, iterative multiuser detection or interference cancellation followed by decoding is performed to approach maximum likelihood (ML) receiver performance without excessive complexity. But for coded CDMA systems, even this iterative receiver may lead to complicated algorithms especially when the number of users is large. Typically with CDMA, the complexity of multiuser detection or soft interference cancellation algorithms grows in polynomial form with the number of users/user terminals. On the other hand, similar to IDMA, SCMA lends itself to a simple chip by chip detection algorithm whose total complexity grows only linearly with the number of users. Further, uncoded SCMA systems perform at least as well as and usually better than uncoded CDMA, and the performance gap between the two classes of schemes grows bigger for heavily loaded systems. Further, in conventional burst mode communication systems, a transmitter transmits burst mode signals at a certain frequency, phase and timing, which is received by a receiver through a communication channel. In conventional burst mode communication systems, it is necessary to quickly estimate various parameters of the received bursts as they arrive. These parameters include detection of the presence of a burst (start time), frequency, initial phase, timing and amplitude. In typical burst transmission systems, a unique word is used to facilitate the identification of the beginning of a transmitted burst and the determination of phase offset, by the receiver. The term “Unique Word” (UW) refers to a known, pre-determined pattern (known a priori to the receiver) that is transmitted at the beginning of each burst, whereby the receiver detects the UW and synchronizes with the received bursts (i.e., the receiver estimates the burst parameters based on the detected UW). For classical TDMA systems, the same UW is used by all of the terminals. While the complexity of SCMA grows only linearly with the number of users, however, with larger systems (e.g., having upwards of tens or hundreds of thousands of user terminals), SCMA system implementations can become relatively complex with each user/user terminal having a distinct scrambling signature. What is needed, therefore, is an approach for an SCMA system that scales more efficiently, and in a relatively less complex manner, to support a relatively large number of users/user terminals. Some Example Embodiments Embodiments of the present invention advantageously address the foregoing requirements and needs, as well as others, by providing an approach for an SCMA system that scales more efficiently in a relatively less complex manner, whereby individual terminals utilize respective assigned unique words and the receiver correlates received signal bursts against these UWs, which supports larger numbers of users/user terminals. Example embodiments of the present invention provide a new SCMA multiple access approach that facilitates random access to a communications channel by a network of terminals in an efficient manner without prior coordination. In accordance with such example embodiments, unique words are respectively assigned to individual terminals, and each terminal utilizes its assigned UW for each transmitted burst. At the receiver side, a receiver correlates the received signal bursts against these UWs to determine whether one or more terminals is accessing the channel and the number of terminals accessing the channel (assuming there is at least one), to identify the scrambling signature or initial vector each such terminal is utilizing to access the channel, and to synchronize with (e.g., determine the timing and phase of) each individual received modulated signal for proper demodulation and decoding. By way of example, a moderately sized set of UWs is assigned to the terminal population, where each different UW is associated with a respective scrambling signature (or, in the case of the use of the same scrambling signature with a different seed or initial vector, each different UW is associated with a respective initial vector) for the scrambler. Accordingly, a receiver separates overlapping transmissions from multiple terminals at the same frequency and the same time slot, based on a UW correlation process employed to detect the transmitted UWs in parallel and thereby identify the number of terminals accessing the channel and the scrambling signature/initial vector of each such terminal, and to synchronize with each individual received modulated signal for proper demodulation and decoding. In accordance with example embodiments, a communications terminal comprises and encoder, a scrambler and a modulator. The encoder is configured to encode a source digital data signal to generate an encoded signal, wherein the source digital data signal comprises a source bit stream. The scrambler is configured to scramble the encoded signal based on a scrambling signature. The modulator is configured to modulate a received sequence of data frames to generate a transmission signal for transmission via a random access channel of a wireless communications system, wherein each data frame comprises a data payload, which includes a block of the scrambled encoded signal, and a frame header, which includes a start of frame (SOF) sequence associated with the scrambling signature. The use of the SOF sequence for each frame of the sequence of data frames provides a reference for synchronization on frame boundaries and serves to designate use of the associated scrambling signature for descrambling and decoding the respective data payload of the frame. The use of the SOF sequence for each frame of the sequence of data frames serves to distinguish between the data frame and at least one data frame originating from a further communications terminal, transmitted via a common time slot of the random access channel, for which a different scrambling signature was used to scramble a respective encoded signal thereof. In accordance with further example embodiments, a multiple access communications scheme is provided. A source digital data signal is encodes to generate an encoded signal, wherein the source digital data signal comprises a source bit stream. The encoded signal is scrambled based on a scrambling signature. A received sequence of data frames is modulated to generate a transmission signal for transmission by a communications terminal via a random access channel of a wireless communications system, wherein each data frame comprises a data payload, which includes a block of the scrambled encoded signal, and a frame header, which includes a start of frame (SOF) sequence associated with the scrambling signature. The use of the SOF sequence for each frame of the sequence of data frames provides a reference for synchronization on frame boundaries and serves to designate use of the associated scrambling signature for descrambling and decoding the respective data payload of the frame. The use of the SOF sequence for each frame of the sequence of data frames serves to distinguish between the data frame and at least one data frame originating from a further communications terminal, transmitted via a common time slot of the random access channel, for which a different scrambling signature was used to scramble a respective encoded signal thereof. In accordance with example embodiments, a further multiple access communications scheme is provided. A transmitted signal is received via a random access channel of a wireless communications network, wherein the transmitted signal originated from a first communications terminal. A first start of frame (SOF) sequence of the transmitted signal is identified, and synchronization is attained on a frame boundary of a first data frame associated with the first SOF sequence. A first scrambling signature is determined based on the identified SOF sequence, and the first data frame is decoded using the determined scrambling signature. The first SOF sequence serves to distinguish between the respective data frame and at least one data frame originating from a further communications terminal, transmitted via a common time slot of the random access channel, for which a different scrambling signature was used to scramble a respective encoded signal thereof. In accordance with example embodiments, a system comprises a first communications terminal and a second communications terminal. The first communications terminal comprises a first encoder, a first scrambler and a first modulator. The first encoder is configured to encode a first source digital data signal to generate a first encoded signal, wherein the first source digital data signal comprises a first bit stream. The first scrambler is configured to scramble the first encoded signal based on a first scrambling signature. The first modulator is configured to modulate a received first sequence of data frames to generate a first transmission signal for transmission via a random access channel of a wireless communications system, wherein each data frame comprises a data payload, which includes a block of the scrambled first encoded signal, and a frame header, which includes a first start of frame (SOF) sequence associated with the first scrambling signature. The second communications terminal comprises a second encoder, a second scrambler and a second modulator. The second encoder is configured to encode a second source digital data signal to generate a second encoded signal, wherein the second source digital data signal comprises a second bit stream. The second scrambler is configured to scramble the second encoded signal based on a second scrambling signature. The second modulator is configured to modulate a received second sequence of data frames to generate a second transmission signal for transmission via the random access channel of the wireless communications system, wherein each data frame comprises a data payload, which includes a block of the scrambled second encoded signal, and a frame header, which includes a second start of frame (SOF) sequence associated with the second scrambling signature. The use of the first SOF sequence for each frame of the first sequence of data frames provides a reference for synchronization on frame boundaries and serves to designate use of the first scrambling signature for descrambling and decoding the respective data payload of the frame, and the use of the second SOF sequence for each frame of the second sequence of data frames a reference for synchronization on frame boundaries and serves to designate use of the second scrambling signature for descrambling and decoding the respective data payload of the frame, even where at least one frame of the first sequence of data frames and at least one frame of the second sequence of data frames are received in a common time slot of the random access channel. Still other aspects, features, and advantages of the present invention are readily apparent from the following detailed description, simply by illustrating a number of particular embodiments and implementations, including the best mode contemplated for carrying out the present invention. The present invention is also capable of other and different embodiments, and its several details can be modified in various obvious respects, all without departing from the spirit and scope of the present invention. Accordingly, the drawing and description are to be regarded as illustrative in nature, and not as restrictive.
3.5625
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Researchers collect fish using backpack electrofishing. Image courtesy South Carolina Department of Natural Resources The problem of invasive species is a slippery one for fisheries managers. One of the most notorious invaders, Asian carp, now dominates large portions of freshwater in the central U.S., and keeping them out of the Great Lakes could cost upward of $18 billion, according to a recent study by the U.S. Army Corps of Engineers. There are a number of preventative measures in place to keep invasives from entering new waters. But at present there are few measures that fisheries managers can use to get rid of invasive fish once they’ve established themselves: basically, toxic chemicals, or targeted fishing. But a better remedy may be as simple as a small dose of electricity. That’s the idea behind a recent study, which found that electrically charged wands can help eradicate invasive fish in small streams with less collateral damage to the ecosystem. Battle of the Trout For years, ecologists in Montana have been tracking an underwater fight. Brook trout, an invasive species in the Upper Missouri River Basin, have increasingly replaced the native westslope cutthroat trout. The two species compete for scarce food, and brook trout appear to be winning. This concerns local ecologists because populations of the westslope cutthroat trout, Montana’s state fish, are in steep decline. The standard response in other waterways has been to use toxic chemicals called piscicides. But these chemicals are problematic – they kill native and invasive fish alike, and also kill many of the aquatic insects that fish eat, says Reuben Goforth, a professor at Purdue University. So the Montana team wanted to try a better way. They turned to backpack electrofishing, a technique that’s widely used at present to sample fish populations. It works like this: Researchers carry backpacks with electricity generators powered by 24-volt batteries. Those generators are hooked up to wands that carry a flow of positive electric charges. (If you’re imagining a setup that looks like the Ghostbusters proton pack, you’re not far off.) The researchers dunk the wands into streams. Soon, fish begin to cluster near the positive charges, a phenomenon known as galvanotaxis. With both natives and invasives gathered, the researchers send an electric burst of 100 to 600 volts into the water, which stuns the fish. The researchers net the temporarily immobilized fish, separate out the invasives (which can be cooked) and return the natives to the stream. Proof of Concept The researchers used this technique on four streams in the Montana Rockies over the course of 13 years. They performed the electrofishing twice yearly: in the fall, when the fish spawn, and in the early winter, when they congregate. Today, after killing an estimated 17,000 invasive fish, the researchers say they have completely eliminated invasive brook trout from the treated stream segments, which ranged in size from 0.3 to 1.8 miles. And they did so without having to use piscicides. “The cost we figured for electrofishing removal was comparable to piscicides in these smaller streams,” says Brad Shepard, the study’s lead author. The results were published in September, in the North American Journal of Fisheries Management. Other Pesky Invasives Shepard says that backpack electrofishing could be used to fend off any invasive fish in smaller streams—including escapees from fish farms. Farmed Atlantic salmon, he notes, have escaped from their pens and been found in streams on Canada’s west coast. Researchers fear that the fish could crowd out native Pacific salmon. Backpack electrofishing could be used in spawning runs to weed out the Atlantic salmon. Asian carp could also be dealt a punch from electrofishing. Purdue’s Goforth has caught numerous Asian carp with boat-mounted electrofishing gear. But because the fish are rarely found in small streams, backpack electrofishing wouldn’t as be as effective as larger versions of the technology, he said, such as the boat-mounted version. So, backpack electrofishing might not be the key weapon against Asian carp. But if you’re a weekend trout fisher, you might consider ditching your fishing rod. A little jolt of electricity could net you a few more dinners.
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Pharmaceuticals in Drinking Water? The problem of contaminated tap water in the U.S. goes well beyond Flint—and also beyond lead. There are many more toxic chemicals in our drinking water that we like to believe. Communities in New York, New Hampshire and Vermont recently found elevated levels of PFOA, a suspected carcinogen, in their water supplies. PFOA, or perfluorooctanoic acid, is a synthetic perfluoroalkyl chemical used to manufacture nonstick pan coatings and water-resistant clothing. And, even more recent is the finding that water discharged from Burlington’s wastewater treatment plant into Lake Champlain—the source of drinking water for tens of thousands of people in the Burlington area—contains concentrations of pharmaceuticals high enough to reflect demographic shifts in the city. The presence of pharmaceuticals in drinking water from different U.S. areas has been know for more than a few years. A report publicly released in 2011 by the U.S. Government Accountability Office revealed that drinking water in some metropolitan areas contains pharmaceuticals, and raised concerns about their potential impact on human health. According to the World Health Organization “Pharmaceuticals are synthetic or natural chemicals that can be found in prescription medicines, over-the-counter therapeutic drugs and veterinary drugs. Pharmaceuticals contain active ingredients that have been designed to have pharmacological effects and confer significant benefits to society. Pharmaceuticals can be introduced into water sources through sewage, which carries the excreta of individuals and patients who have used these chemicals, from uncontrolled drug disposal (e.g. discarding drugs into toilets) and from agricultural runoff comprising livestock manure. They have become chemicals of emerging concern to the public because of their potential to reach drinking-water.” Emma Rosi-Marshall, a scientist at the Cary Institute of Ecosystem Studies and lead author of a study published in 2013 on the effects of pharmaceutical pollution on aquatic life and water quality, said in a press release: “Pharmaceutical pollution is now detected in waters throughout the world. Causes include aging infrastructure, sewage overflows, and agricultural runoff. Even when waste water makes it to sewage treatment facilities, they aren’t equipped to remove pharmaceuticals. As a result, our streams and rivers are exposed to a cocktail of synthetic compounds, from stimulants and antibiotics to analgesics and antihistamines.” Results from a study published this year in the journal Science of the Total Environment show that water samples from private wells on Cape Cod are contaminated not only by perfluoroalkyl chemicals and flame retardants, but also by a dozen different pharmaceuticals. The researchers found that sulfamethoxazole, an antibiotic used to treat urinary tract infections, and carbamazepine, a drug used to treat seizures, nerve pain, and bipolar disorder, were among the most common pharmaceuticals detected. The researchers also found that the pharmaceuticals were present at concentrations orders of magnitude lower than those found in a therapeutic dose. However, Laurel Schaider, the study lead author, said in a press release: “But that doesn’t necessarily mean there’s nothing to worry about. Drugs are intended for specific uses and can have side effects, and we don’t give certain medications to pregnant women or children because the developing body is very sensitive.” Another concern is that people might have allergies to some of the drugs that contaminate the water. Antibiotics, for example, are known to cause allergic reactions in susceptible people. These reactions can be severe—they include symptoms that range from hives and wheezing to the potentially life-threatening anaphylactic shock. In the press release mentioned above, Schaider also said: “People often don’t think about where their tap water comes from. But it’s really important that they do and that they take steps to make sure it’s safe.” 24 Comments I am surprised to read that pharmaceuticals are so rampantly infesting our water, not because of the infestation itself, but because it may have an effect on our well-being. I recall when I was younger, and the neighborhood boys would try to persuade us that our drinking water was actually urine, filtered out. While that’s probably not actually how it works, it’s peculiar to me that trace amounts matter to us, rather than just animals. I wonder if there’s anything to be done about this, besides “damage control.” Can we clean the water that’s routed through our sewers and into our drinking glasses? As an employee of a local, independent pharmacy, surprisingly, I see the threat of pharmaceutical-contaminated water frequently. I cannot count the number of times a patient has entered into the pharmacy with bags full of expired prescription medications or drugs he/she is not taking anymore looking for a proper disposal method. We are thankful these patients come to us and ask because most people simply flush their medications down the toilet or sink. Having active ingredients from medications in our drinking water is a major health concern with risky consequences, so the FDA has a method that does not effect our water. The problem is, however, is not a lot of people know this or do the research — they simply flush the pills because it is easier. According to the FDA, you can safely dispose of medications in your household trash. They ask that you mix the medications with either coffee grounds or kitty litter, place it in a sealed bag, and simply throw it away with your garbage. If you do not feel comfortable using this method, the DEA holds national drug take-back programs where collection sites (i.e, police stations) are set up for the safe disposal of medications. This was a great informative read, and one that does not come as a surprise to me. Please keep in mind that this is going on in a country in which it is hard to find bottled water with simply just the ingredient “water” written on it and nothing more. Today’s bottled water can contain magnesium chloride, sodium chloride, and magnesium sulfate. This seems a bit excessive for such a simple beverage as water. There are claims that these ingredients are used to enhance the taste of water or to add minerals to the diet. In addition to this, the FDA allows small amount of contaminants in bottled water, as long as it is kept under a certain level. This includes bacteria called coliform, arsenic which we have spoken briefly about in class, and phenols. I challenge you to read a the ingredients on a bottle of water next time you drink. I think this is a definitely an issue that should be tended to quickly, no matter where it is occurring. I agree with many of the posters that this could be contributing to our problem of antibiotic resistance. One of the most common pharmaceuticals detected, sulfamethoxazole, can further aggravate conditions for those with autoimmune disorders. My question is what is being done to prevent this from happening? Even though the pharmaceuticals are in small amounts “deemed” harmless now, in the future it could definitely pose a problem. Considering our lack of fresh drinking water available, we should do what we can now to care for it the best we can. The issue concerning water contamination just as affrometioned in the article does indeed go beyond Flint, Michigan. Improper usage or disposal of many of our daily products have been shown to also be a contributory factor. And the idea that some pharmaceutical products makes its way to our drinking water is alarming. Pharmaceutical drugs or products contain some chemicals that when not handled or used correctly could lead to multiple effects. And knowing this same toxic substances makes its way to freshwater is also concerning not only for current generation but also for the future generation. I believe just as the article states educating people about large about the potential risks associated with contaminated water would in turn I believe raise awareness and lead to people taking action in hope of reducing the risks. There is a famous french proverb by Olivier Blanchette which states that “l’eau est source de vie” , meaning that water is a source of life, because we, as humans, can live without anything but water. When growing up with this in mind, and after reading that article, the only thing I can think of is how water that is supposed to give us life, be now contaminated will all the pharmaceuticals that can lead us to death? Yes! I say death because when I read the article I am not thinking about the fact that the doses present in the water are mild. I just think about how much water we have been consuming since we are born, and how that mild dose everyday is becoming worst as we go. Consequently, the only thing that I see now is how people can protect themselves from now on because the government does not seem to care about the population. The only measures that are found are related the pharmaceutical companies and the FDA such as: improve the design of the drugs such as they can be eliminated in the body and not go into excretion, FDA should be harsh regarding the approval of drugs, produce only necessary drugs. I found this feasible, so I do not understand why they are still not done yet. Because the measures are only related to them, but it seems that they do not want to take actions, I believe that they should at least find measures that could be applied to the population, to us. Consequently, we can have the choice of whether or not we want to take our own actions, and whether or not we want to save ourselves. That would be more fair to us, and it could save us some damages along the way. It was also very alarming to me to find out that the water we have been consuming contain such pharmaceuticals mentioned in this post. This was the first instance of me reading about water contamination with pharmaceuticals. According to the article, the U.S. government only took accountability in recent year and admitted the drinking water in some metropolitan are contain pharmaceuticals and raise some concern over potential harm to the population. Just as the flint crisis I feel like they are down playing the severity. I believe there need to be an extensive study needs to be done into water contaminations not only in metropolitan areas but other areas. Nevertheless, as you mentioned we really don’t know what kinds of side effect we will be facing with past and potential future exposures unless something can be done about it. In this study, a new analytical technique was used to effectively trace Carbamazepine, a anti-epileptic drug, and its metabolite found in urine that is recalcitrant compound. This drug has a high absorbance by crops in farms from contaminated underground water. The technique provided a selective and sensitive quantifications of the Carbamazepine and its metabolite in urine in the environment. This allow for a previously difficult detection in sewers to become a lot easier for cleanup efforts in the future. In searching up more studies on pharmaceuticals clean up I have noticed not a lot of study is being done to improve this issue. I am not sure f this is because pharmaceutical contamination of drinking water isn’t considering a priority or not but neglecting such a huge public health concern is only going to hurt us in the long run. This article talks about the presence of pharmaceuticals within the common person’s drinking water, which not only raises concern about the health effects on those who have consumed it, but also the length of time this problem has been present. Despite the drugs have been found in low concentration that are below the normal prescribed amounts , this still creates a form of danger to those drinking this water due to not only the mixture of them , but also take into consideration possible allergens to medications and what prolonged exposure can do to people. It simply raises flags that this situation has occurring for the past few years. It raises questions of the integrity of the United States water filtration and purification system, where else problems like this can be occurring without our knowledge. Review and possible remediation of water centers may be in the immediate future. There are so many chemicals polluting our drinking water today. The EPA requires drinking water treatment plants to test for up to 90 different contaminants and of that 90 surprisingly pharmaceutical drugs are absent from that list. This is frightening because there has been a growing concern regarding pharmaceutical drugs being found in our drinking water. A majority of these drugs are getting into our water because of people disposing of their medicines in the toilet. Even after FDA advised that people mix them with kitty litter or coffee grounds before putting it in the trash or dumping it at a collection site, people still result to flushing their prescriptions down the toilet. One thing I found interesting was that our body metabolizes only 90% of drugs that we intake, so the other 10% is either excreted through waste or sweat so, either way, these drugs are going to affect our water. However, if people can start disposing of their drugs the safe way as FDA advised that would minimize a majority of the drugs present in our water today. People drink water all the time so we cannot solely rely on wastewater treatment plants. We do not know how these drugs are affecting us, but the potential of risk is still present, and we cannot take that chance especially when pregnant women, the elderly, and young kids are drinking this water. Some believe that the problem could be solved if doctors lowered the dose of medication. I personally disagree with this because reducing the dose of medication for a patient might not be beneficial for them. Some people suffer illnesses that require a higher dose of medication and just because the dosage is lowered doesn’t mean people will stop flushing their medicine down the toilet. I think the best solution is to educate people about our drinking water, the different things that are currently affecting it, and ways that we can prevent people from experiencing negative effects from our water. If the antibiotics that are found in drinking water are still relatively active, the potential for the antibiotics to increase antibiotic resistance can also be an issue. Being that we already have an ongoing problem of antibiotic resistance, the possibility of drinking water contamination by antibiotics perpetuating the problem is of high concern. Unfortunately, antibiotics are not the only pollutant capable of causing health concerns. Some of these pollutants are not even regulated. It should also be noted that a lot of the contaminants found in water are not only a result of human pollution. A lot of chemicals occur naturally such as arsenic, manganese, mercury, and selenium. Granted, these elements do not do much to your health at low concentrations, but the problem is the increasing concentrations of these chemicals as a result of current industrial waste disposal procedures. Part of the problem is the lack of awareness of the issue. If you were to ask anyone if they know of the variety and amounts of chemicals that are present in their drinking water, most people would say no. This lack of awareness stems from the fact that the effects of water pollution are not readily apparent to people in developed areas. The problem also extends beyond humans into the ecosystem. From my experience, most people do not care about what happens to animals and plants in the wild as long as they get what they need. This attitude is also very common within the government when they are making the choice between money or conservation and sustainability. To a lot of people, if the government is not doing anything about water pollution, then why should they? Therefore, if prevention is not viable then we may have to resort to developing filtration systems that strive to reduce the amount of toxic chemicals in water and to enforce stricter regulation procedures. Reading this blog post and taking an overall look at the sustainability model that we have been talking about in class, it seems to me that there is one common problem tying the water crisis together. That problem is a lack of concern, knowledge, or to simply put it ignorance on our part. The water crisis in Flint exemplifies the lack of concern on the part of city officials. By trying to cut cost, they failed to understand the consequences of their actions and now the lives of people have to pay the price. The situation presented in this blog about how pharmaceuticals are now detected in the drinking water highlight our ignorance on proper drug disposal. One possibility to stop this problem is education. We need to educated people on the potential hazards of throwing chemicals and unused drugs away and also the proper way of disposal. Although it is stated in the blog that the concentrations of these pharmaceuticals are at low concentrations, it should be pointed out that having all these different drugs with different functions mixed together in drinking water could affect us and animals living in their environment. For example there have been drugs that have affected fish by alternating their eating habits and anxiety. With that being said, Eloy I agree with your statement that you made about how people do not care about what happens to plants or animals as long as they get what they want. Unfortunately some people really don’t care about this situation until it personally affects them whether it’s their business or their own personal health. Until then these people will continue with their habits which will undoubtedly have a profound impact on the lives of other people and the animals in the environment. In order to counteract that there needs to be new treatments in placed to treat pharmaceutical contaminated water. Current treatment approaches fail to remove most of the pharmaceuticals in water. There are new technologies that can help remove the pharmaceuticals in drinking water. One them is using carbon filters with uses activated carbon. One study has shown that is has helped removed 90-98% of pharmaceutical residues. Another new treatment is onzonation. Through this treatment electron rich structures in molecules are attacked due to ozone being a selective oxidant. Studies have shown that up to 95% of pharmaceutical residues can be removed. It is quite disturbing that not only are some areas of the United States, as well as those around the world, have an issue with emptying aquifers but the remaining water and water in the system used for drinking water is contaminated with chemicals and pharmaceuticals. Water could be argued to be the most important element in existence, especially for life. Yet somehow it has become a dumping ground for multiple dangerous compounds without regard for the consequences on human, animal and environmental safety and development. It is very unsettling that human beings have ruined our natural resources due to carelessness, greed and side effects of developing society. As of now, many scientists are attesting to the danger and potential threats looming with regards to the chemicals and pharmaceuticals in the water. According to the World Allergy Organization, infant allergies are on the rise, mostly those associated with food. This makes sense, since contaminated water is used to harvest and grow crops used to feed citizens. While the long term effects of the water contamination on human development and immunity is far from being understood, it is not a leap to be concerned that the effects of even small “non-therapeutic” dose of medication can be detrimental those humans especially infants. While the contamination has occurred and there is not much can do regarding that aspect of the problem, unless we had a time machine, we can prevent further contamination and develop methods for obtaining water from sources other than the bodies of water that are contaminated until they can be properly cleaned. We should take note of inventions such as those by Arturo Vittori. He invented a special tower designed to absorb water from the atmosphere. In order to protect our immune systems, future generations and the rising threat of antibiotic resistant bacteria, filtering and ensure our drinking water is clean should be one of the highest priorities! Although the chemicals in the water may be at a level that the human body can sustain, what will become of us as time progresses? Will our bodies still be able to withstand any harmful effects of this contaminated water? Scientists have already proven that chronic exposure to the low level of drugs in Lake Monroe of Indiana, the main water reservoir, causes lower reproduction rates and embryo development issues in zebra fish. Yes, fish and humans are not the same, but this does provide us with a glimpse of what could be if we don’t take steps to resolve this issue. Experts recommend that pharmaceutical companies find novel ways to dispose of their waste and even change the formulas of drugs to accommodate the water treatment process, which does not cater to many chemicals found in pharmaceuticals. This article was about pharmaceuticals being in the publics drinking water, which is a scary thought. The article does mention the concentrations being lower than the therapeutic dose. Some people might find that comforting but nevertheless people are still ingesting it. I enjoyed how the article ends on Schaider saying people need to take steps in making sure the water they drink is safe. Water is a universal solvent, so it has the ability to dissolve almost anything it comes in contact with. With this in mind, although water may look safe there is a chance it is not. The first way to be safe is to have your water tested. This can be done by the local water supplier or a state- certified lab. It’s also possible to test the water yourself. (2) At home test kits can test for: Bacteria, lead, pesticides, nitrates and nitrites, chloride, hardness, and more. The Water Quality Association has a few methods for point-of-use solution to treat water before consumption. One is the activated carbon, that filters out benzene, various pesticides, lead, and more. (1) It is recommended to at least test for coliform bacteria and nitrates because they are tied to intestinal illnesses and blue baby syndromes for infants. Knowledge is power, so the next thing is to get informed on the different contaminants that might be in your water. This way it can be known what device can protect you from them. 1. At the Faucet. (n.d.). Retrieved April 26, 2016, from https://www.wqa.org/Improve-Your-Water/Solutions/At-the-Faucet 2. How to tell if your water is safe | BabyCenter. (n.d.). Retrieved April 26, 2016, from http://www.babycenter.com/0_how-to-tell-if-your-water-is-safe_469.bc?showAll=true At least with the rooting around I’ve done on various sites, it seems like the levels of these pharmaceuticals are not high enough to cause any acute problems, but I think that this post and the linked article do raise valid concerns for a potential disaster in the future. I also wonder if there is a chance that the antibiotics that are being put into water sources will contribute to the buildup of resistant strains that will affect anyone who associates with the water source. While there is much work to be done in figuring out a proper industrial disposal of pharmaceuticals, it sounds like what will have the most immediate and impactful effect is for the general public to properly dispose of old medications. The FDA has a list, which they are continually revising, of medications that are considered safe to be flushed down the toilet (1). The FDA even recommends putting the drugs in a sealable plastic bag with coffee grounds, dirt, or kitty litter (2). Drugs that are not safe to flush can often be returned to local police departments, or some other government building, for proper disposal. I’ll even put a list of these places for the state of Georgia below (2) Drug-resistant bacteria were the first thing that popped in my head too after reading this article. Not only are antibiotics already misused a lot (sometimes with wrong prescriptions or people just taking them for any little headache or even a viral infection!), they are also getting introduced to our water sources? This can eventually lead to a recipe for some super-resistant bacteria. According to Wright, S. anti-biotic resistant urinary bacteria are already on the rise just from trimethoprom-sulfamethaxazole prescriptions alone. I agree with informing the public and giving safer methods of disposing the medications. Relying on the public to fix this problem totally might not be super efficient though as non-compliance has always and will probably always be an issue. In addition to informing the public, I think the pipelines used for transporting our water should be augmented in a way that there would be no cross-contamination. Better water recycling and purifying techniques could also be used in addition to the public help and better pipes. The advances in industry and medicine have been widely beneficial to mankind but the unseen consequence of our improvement has polluted our water supply. These contaminants include “antibiotics, hormones, contraceptives and steroids.” The U.S. Geological Survey found these pharmaceuticals in 80% of the rivers and streams they surveyed since 2000. The number has likely increased since then. The improper disposal of drugs has been a concern and been researched by the Citizens Campaign for the Environment (CCE). They state that the “possible health concerns include hormone disruption, antibiotic resistance, and synergistic affects” as well as the “alteration of behavior and reproductive function of fish and mollusks” due to antidepressants. These are just a few known outcomes; the danger comes from the side affects and the surprise cocktail of drug interactions. The lack of information about proper disposal of these drugs has lead to this epidemic. These problems can effects pregnancies, childhood development and other wildlife that unknowingly utilizes contaminated water sources. The FDA’s guideline for proper disposal is to locate take-back programs or to throw the drugs in the trash and not down the toilet. The drugs should also be mixed with unsavory substances to make them less appealing to children and pets and to be put in bags to prevent leakage. The water supply needs more careful monitoring and programs to actively remove these substances. Without awareness and actions we are doomed to be in fear of the water in our faucets. The original article emphasizes the newly prioritized and drastic effects pharmaceutical drugs being released into the environment. Specifically, these effects and concerns were focused on the human population. I’m not a huge animal-activist but I hate to see anyone or anything taken advantage of or left-out. So not including animals or wildlife organisms in this conversation would be unjust. We do not live our entire lives outdoors and in the actual environment like animals do. In fact, wildlife is exposed to the contaminated water and environment for much longer periods than humans are. We have treatment plants and precautions to help lessen the amount of pharmaceutical drugs in our water or food, but animals do not have this luxury. They take food and water as it comes. So I was interested to learn about the effects these released drugs had on other forms of life, besides our own. A study was done on the environmental effects, and a section was devoted to animals. Changes in a demographic can apply to animals, not just humans as mentioned in the article. Insects affected by pharmaceutical drugs can be changed physiologically and behaviorally. Other drugs can affect fish development and fertility. Antibiotics have the ability to affect animals that live in the soil by off-setting the sensitive ecosystem and environment. So not only are we depleting the Earth of freshwater, but we are ruining what we have with more than just lead like in Flint, Michigan. We are drastically out-numbered by other forms of life. Insufficient and contaminated water will affect these organisms, but humans definitely use the Earth more than our counterparts. This takes us back to what we discussed in class for two weeks. As the dominant users of Earth’s resources, we have to learn moderation AND “system thinking.” We already know the damage waste and apparently pharmaceutical drugs can do. Now we need to accept the problem, and make a commitment to fixing it. Some companies and workers have already started by controlling disposal of labeled pharmaceutical drugs, such as hospital-waste water. If the sources of pharmaceutical waste were better controlled, we would have less in our water. If we don’t make an effort to stop overusing and contaminating water, not only will we lose one of our most precious resources, but also many sources of food and organisms that keep us alive. Tanderson makes a valid point in mentioning how not only are the chemicals negatively affecting the human population but they are also affecting the animals. One thing that this made me consider is how humans implement this behavior. In addition to the chemicals that animals are exposed to in the environment, animals are also being used as a vector to bring more pollution to the environment, affecting animals and humans. Of course, the animal is not at fault but the humans are, as we continue to use animals in research and dispose of the waste in the environment. According to the link below, millions of animals are used in research and they produce an abundance of waste. They produce food waste, chemicals, diseases, even viruses. Also ground water and air are polluted due to incineration and soil pollution. So, not only are animals being affected by the pollution, but they are being used by humans to cause even more pollution. Going down this path, pharmaceuticals won’t be the only thing that we have to worry about being in our drinking water. I’m sure while reading this article many arrived to the supporting evidence in the article that mentioned that researchers found that pharmaceuticals were detected in lower concentrations than the therapeutic dose and thought, “then why is pharmaceutical contamination in water such a big deal?” Considering there are a significant amount of pollutants found in water like lead and mercury with more serious side effects, I know I did. However, I then arrived to the part of the article that mentioned a concern for those with drug allergies that could come across a drug that can trigger an allergic reaction in their contaminated water. According to an Associated Press investigation, antibiotics, anti-convulsants, mood stabilizers and sex hormones have been found in the drinking water of at least 41 million Americans. Keeping in mind common drug allergies to drugs such as penicillin-type antibiotics, sulfonamide-containing antibiotics, NSAIDs such as aspirin or ibuprofen, etc., it is important to note the potentially serious threat being posed on those with drug allergies consuming drinking water with possible traces of these drugs. Although no major health effects have yet been detected by the EPA, the matter should not be overlooked due to the possible allergic reactions that can arise by pharmaceutical contaminated water potentially causing sudden side effects such as hives, anaphylactic shock or death that may arise from simply drinking a cup of tap water. This is more so something to fear because it is not easily detectable and even more worrisome because water pollution by pharmaceuticals has been a concern for decades and has proven unreasonable to completely eradicate due to the pharmaceutical contamination of wastewater through feces, consumers flushing pills down toilets and also because most water treatments fail to remove all drug residue. It is important to note that not only is this contamination making its way into our drinking water, but also to rivers in which the fish we consume inhabit. After learning about the potentially serious long term health effects posed by consuming lead contaminated drinking water, I believe it is important to research the potential long term effects of consuming pharmaceutical contaminated drinking water, more specifically, the unknowing consumption of drugs that are not specifically prescribed to us through pharmaceutical contaminated water. Perhaps increased antibiotic resistance may arise by the continuous consumption of small traces of antibiotics or sudden mood swings may arise from the discontinuous consumption of antidepressants or even a serious drug interaction may arise from a drug unknowingly consumed through drinking water and a prescription someone may take daily. This is definitely one to look into. The fundamental element of survival for all creatures including ourselves is water and its scarcity and contamination is something we should put as top priority in solving. Freshwater has already been depleted because of global warming and air pollution but now we have to face the issue of pharmaceutical contamination in our drinking waters. Pharmaceuticals is indeed a potential need for the entire human population as it can save our lives or helps us maintain a stable lifestyle. However, these pharmaceuticals may not only contaminate our drinking waters but also waters in agriculture or wild animals we feed off of. Pharmaceuticals present in water may show defects in animals or the destruction of agriculture. When we consume these contaminated food or agriculture, we may develop certain diseases or illnesses. However, researchers are now trying to change the chemical structures of pharmaceuticals so they can be degraded in the body and in sewage treatment system before contaminating our waters. They’ve chosen propranolol for their study and changed its chemical structure but still has the function of treating heart problems and high blood pressure. This could be a potential strategy to reduce further pharmaceutical contamination in our drinking water in the future. The perpetuating problem with low concentrations of pharmaceuticals found in [private] wells is a complex issue that requires a collaborative effort. Although the concentrations measured by the researchers were significantly lower than the therapeutic dose, the current water crisis should act as a catalyst in recognizing the actual significance of these low concentrations of pharmaceuticals found in a water source that is almost entirely depleted. Furthermore, researchers have observed the extensive influence pharmaceutical-contaminated water has on important ecological systems that may result in detrimental consequences for higher trophic levels. The concentrations of pharmaceuticals in water can only increase if the causes for these issues are not addressed as the availability of necessary freshwater is diminishing right before our eyes. Domestic drinking water wells are often more shallow, increasing the chances of higher pharmaceutical concentrations in the water. Domestic wells are used in communities that are served by onsite wastewater treatment systems, providing source for pathogens and chemical contaminants in ground water in areas with high septic system density. The causes for these issues include aging infrastructure, sewage overflow, agricultural runoff and improperly equipped mechanisms of purifying drinking water. To put it blunting, human existence bears the fault for the current global climate and water crisis. Urbanization, increasing population, deforestation, and overall zealous misuse of the Earth’s resources without regard to the consequences of an increasing population in demand of resources that are being depleted at record breaking rates- play a detrimental role in our current global climate and water crisis. Fortunately, we come equipped with the means of addressing these issues; however, I understand that this is a more complex issue that requires significant financial support, education on the long term impact of pharmaceutical therapy and possible preventative measures, placing importance in knowing where your water is coming from and how it is being purified, and electing official representatives who place high priority in implementing efficient regulations for optimum water quality of the wells and aquifers that remain viable, as well as the global climate as a whole. In a collective effort, we can help minimize the large carbon footprint that we have already begun to leave. LTran, I agree with your point of view on this issue. Human negligent is absolute to blame for this aquatic pharmaceutical pollution problem that we’re encountering right now. Aside from the pharmaceutical manufacturers and agriculture farms negligently dumping their chemical water waste into the sewage system we also have to take into account the negligent of hospitals and the general public as well. First of all, chemicals can also get into the water from the drugs we use. Our bodies metabolize only a fraction of most drugs we swallow. Most of the remainder is excreted in urine or feces and therefore gets into wastewater. Topical medication such as creams or lotions, the unabsorbed portions of those medications can contribute to the pollution problem when they get washed off. Aside from our unintentional actions, what do you think regarding what people do regarding theirs expire prescriptions medicine? Yes, some of us may probably discard it through the right authority, but many people would just dump the med into the toilet or the trash. These chemicals eventually ended up into the sewer system, and then to our aquatic environment and causing such rising in our marine pollution. Health care institutions are another source of pharmaceutical water pollution. Some hospitals are probably less of a problem than other because their strict protocols regarding unused drugs but many do not. Many healthcare facilities especially nursing homes have often been guilty of flushing medications down the toilet or drain after a patient dies or is transferred to another facility. And the unspoken rules for getting rid of opioid painkillers, which make disposal down the drain an acceptable option, have inadvertently encouraged some nursing homes to dispose of all their leftover medications that way. Problems will continue to rise if we don’t take actions. In my point of view, there are a few different ways I can think of that we as the general public should do to cut down such an issue. First, limit the bulk purchase of over the counter drugs, this way peoples can cut down from discarding their unused medications. Second, use drug take-back programs to take back drugs locally and properly incinerate and discard them. And finally do not discard our medications down the drain and trash. If we can be more mindful regarding our actions, we may be able to create a better cleaner future. The idea that there are pharmaceuticals and other chemicals floating around in our drinking water is of major concern. Even in a developed country such as the United States, we too are facing the reality that our water might not be as safe as we are told. In several states, they have found evidence of chemicals such as PFOA a possible carcinogen and several pharmaceuticals either over the counter or prescribed within the drinking water. We are not aware what interactions or problems may arise with these chemicals present in our water. In the study Occurrence removal and risk assessment of pharmaceutical and personal care products (PPCPs) in an advanced drinking water treatment plant (ADWTP) around Taihu Lake in China, they found that even when using the guidelines for purification techniques there were three chemicals still found in the water. Those were caffeine, roxithromycin, and sulfamethoxazole. Caffeine has several drug interactions and when mixing with your medications it can cause effects such as increased heart rate, low blood pressure, irregular heartbeat, anemia, and can cause a caffeine overdose by increasing its effects (http://www.caffeineinformer.com/caffeine-drug-interactions). Sulfamethoxazole can cross the placenta and is considered a class C in pregnancy which is not safe to take while pregnant (http://www.drugs.com/pregnancy/sulfamethoxazole.html). There must be a reform in the way the water is treated, so that we know we can safely drink the water without worrying about the presence of harmful chemicals.
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Flight helmet A flight helmet, sometimes referred to as a "bone dome" or "foam dome", is a special type of helmet primarily worn by military aircrew. A flight helmet can provide: Impact protection to reduce the risk of head injury (e.g. in the event of a parachute landing) and protection from wind blast (e.g. in the event of ejection). A visor to shield the eyes from sunlight, flash and laser beams. Noise attenuation, headphones and a microphone (except when included in a mask). A helmet mounted display, mounting for night vision goggles and/or a helmet tracking system (so the aircraft knows where the pilot is looking). The design of a flight helmet may also consider: Comfort - including the weight, centre of gravity and provision for cooling and ventilation. Compatibility with an oxygen mask (for high-altitude flight and NBC protection). History of flight helmets In the first days of aviation the leather helmets used in motor-racing were adopted by pilots as head protection. The initial design of early leather flying helmets was adapted during the 1930s to become the type B helmet which enabled the external attachment of radio earphones oxygen masks and removable goggles to protect pilots eyes from the elements. By World War II, an oxygen mask was added to the equipment as planes flew higher where thinner air required a breathable air supply to the pilots and crew. After World War II into the Korean War, the leather headpiece was gradually replaced with a hard helmet needed as head protection during bailing out (and later with high velocity ejection). Also, goggles were replaced by a visor that was incorporated to the helmet and tinted to protect against sun. Current head gear (appears after the Vietnam War) also includes communications equipment (head set and microphones) to let pilots communicate with ground operations and their crew. References External links Images USSR fighter pilot helmet Category:Helmets Category:Aircraft components Category:Aviation medicine Category:Aircrew clothing
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This invention relates to a bicycle shock-absorbing apparatus, and more particularly, to an apparatus that utilizes elastomer polymers instead of springs or the like to absorb a shock from a uneven terrain. A conventional bicycle does not have any shock-absorbing apparatus attached to either the front or rear wheel axle. Therefore, a biker will feel discomfort when passing over an uneven terrain. In addition, long term use on an uneven terrain will damage the bicycle. With the above drawbacks, the bicycle needs to be improved to have better performance. An off-road bicycle (or a mountain bicycle) is popularly used for sport and leisure. Therefore, a safe and trouble-free bicycle is a basic requirement for off- road use. A number of front fork designs have been disclosed for off-road motorcycles. However, a bicycle is quite different to a motorcycle in many ways, such as the momentum of a motorcycle is much greater than that of a bicycle under normal use, as a motorcycle has a greater mass and is used at higher speeds than those of a bicycle. Therefore, simply adapting a current motorcycle shock-absorbing apparatus onto a bicycle is not feasible. U.S. Pat. No. 4,971,344, teaches a bicycle with a front fork wheel suspension that utilizes a pair of telescoping tubes and a spring-loaded valve, so that the latter can regulate the flow of fluid between the pair of telescoping tubes and thus absorb shock from an impact. U.S. Pat. No. 5,094,324, which belongs to the present inventor, also discloses a bicycle shock-absorbing apparatus comprising an inner tube, a valve device, and an outer tube cooperating with a pair of springs and damping oil loops therein for absorbing the shock impact from an uneven terrain. Another U.S. Pat. No. 5,088,705, which also belongs to the present inventor, discloses a bicycle shock-absorbing apparatus comprising an inner tube and an outer tube. An upper spring socket and an lower spring socket are disposed in the inner tube and the outer tube separately. A compression spring is disposed between the spring sockets, oil being filled between the spring sockets. The inner tube is fixedly attached to the upper spring socket and corelatedly actuated with the spring to achieve a shock absorbing effect. However, the above disclosures utilize springs which are apt to loose elasticity in use over a long time. The change of the spring(s) is cumbersome because the spring has to be linked with corelated socket(s) and the damping oil will cause trouble when changing the spring.
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In general, a computer program consists of a sequence of instructions all of which belong to a particular instruction set. At the appropriate time, each instruction is typically loaded into an instruction register where it resides while being decoded and executed. The execution of one instruction normally involves a plurality of steps. In many processors, each of these steps is performed by the execution of a microinstruction which may be stored in a read only memory. Accordingly, for these processors, a stage is required whereby a sequence of microinstruction memory addresses are provided for one instruction. In the prior art, this has been accomplished through the use of hardware logic that decodes the instruction. Commonly, each instruction is divided into a plurality of fields, each field consisting of a single bit or contiguous bits. Examples of fields are format, operation code, address mode, register specification, etc. The number, size, and types of fields may vary within one instruction set. Generally, the hardware decode logic determines the particular format from a delineation field within the instruction and then decodes the remainder of the instruction according to that format. However, when it is desirable to emulate a different processor using a different instruction set, different hardware decode logic is required.
3.703125
4
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Q: grounding, whats its purpose? Some say Ground is just a reference point for measuring voltages, some say ground is a safety device for appliances and some say ground is just a bare piece of metal regardless if its even connected to the actual earth (as in dirt) I have multiple questions about ground: This one is about appliances and is taken from howstuffworks, "Let's say that a hot wire comes loose inside an ungrounded metal case,the metal case then becomes hot so anyone that would touch the case would be fatally shocked. By having a ground wire attached to the metal case, electricity from the hot case will flow straight to ground and will trip the breaker" Can you not be safe just by touching a hot wire alone, granted you don't touch neutral? What if you touch a hot wire then, stick you other finger in the dirt (soil)? So its telling me that the current flow from a hot wire, to the grounding wire-> (connect to some rocks and dirt/poop) is so high, it can trip a breaker? In a DC situation there is no hot wire, and (correct me if i'm wrong) but if I have a 350v Capacitor fully charged, there is absolutely no way for me to get electrocuted unless I touch both terminals. Why doesn't AC behave this way? And how about this: people say step 4 is to ground that wire, How? The car is insulated from the earth All I see is an open circuit. Please help, Thanks! A: The reason this is confusing is because the ideas are confused, mixed up in the word "ground". Sometimes “earth(ing)” is used to refer to the concept of electrically connecting to the earth, allowing “ground” to be used for the concept of “a part of the circuit we consider to be 0 volts”. Some say Ground is just a reference point for measuring voltages That's one of the meanings. You have some device, some circuit, and say that this conductor is 0 V and measure everything else relative to it. If the device is isolated (battery powered and not hooked up to anything else), then it's truly arbitrary, but if you have connections, signal or power cables, to something else — power supply, digital signal, analog audio signal, whatever — then the expected electrical characteristics are generally such that the two devices share the a common 0 V reference — a common ground. (If there's a problem so that one of the devices is causing current to flow along different parts of the system that should be the same “ground”, that's called a ground loop.) some say ground is a safety device for appliances The safety device here is the presence of a connection between the chassis of the device (generally, any exposed metallic parts) and the “ground” conductor of the electric circuit, which is also joined to earth. The safety comes from the idea that if somehow the chassis gets joined to line voltage (“hot”) and current will flow to the “ground” (and perhaps trip a breaker or GFCI/RCD device) instead of through you when you touch it (as you are a higher-resistance connection to earth). some say ground is just a bare piece of metal regardless if its even connected to the actual earth A bare pice of metal is never “a ground” by itself. It's just common, for safety reasons and for electrical design convenience, to design things so that all exposed metal is joined to, or a part of, the circuit's “ground”. Can you not be safe just by touching a hot wire alone, granted you don't touch neutral? If you jump in the air and poke the hot wire, you're certainly safe. If you're touching anything else, like what you're standing on, you might be able to make a circuit. What if you touch a hot wire then, stick you other finger in the dirt (soil)? So its telling me that the current flow from a hot wire, to the grounding wire-> (connect to some rocks and dirt/poop) is so high, it can trip a breaker? Depends on the kind of dirt, and how wet it is. If it's sufficiently conductive, the circuit consists of the incoming electric service (hot branch) → house wiring → you → dirt → service ground connection at the breaker panel → service neutral. (That is if your wiring is like USA wiring, at least.) But safety grounding isn't just about “dirt” — think about the kitchen. You've got electric appliances, salty (conductive) water involved in cooking, possible spills and/or damaged wiring — In a DC situation there is no hot wire, and This is true but misleading. The reason we use the term “hot” with AC only is because AC voltages reverse all the time and so we can't just say “the positive wire” or “the -5V wire” or such. A way to describe either case would be to say “not at 0 V”. (Nominally in that resistance in wiring means that almost nothing is at exactly 0 V.) (correct me if i'm wrong) but if I have a 350v Capacitor fully charged, there is absolutely no way for me to get electrocuted unless I touch both terminals. If you had a 350 V AC power source that was isolated, then you could touch one terminal and be just as fine as in the capacitor case. (Well, mostly fine. Because AC can pass through capacitors, and lots of things are a little bit like capacitors, there could be some current flow, though not much if the other terminal isn't connected to anything and therefore has no opportunity for capacitive coupling of its own.) But your household AC line supply is not isolated — the neutral side is joined to earth — so it is not safe in this way. people say step 4 is to ground that wire, How? The car is insulated from the earth All I see is an open circuit. What they're not showing in the picture is that the “Yours” car is assumed to have the negative battery terminal connected to the car's metal frame, thus completing the circuit in the picture. The reason for that hookup scheme is not anything about the electric circuit itself — it's because the final connection when current starts to flow may make an arc for a moment, and you want that arc to be away from the battery so it doesn't ignite any hydrogen gas that may be in the vicinity. (Mistreated lead-acid batteries electrolyse their water and thus produce hydrogen gas.)
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Navigation using a personal mobile device (such as a “smart” cell-phone) is commonplace, and mostly makes use of satellite based global positioning systems (e.g. GPS). While navigation (i.e., finding one's way from the current position to a desired destination) was the “raison d′etre” for positioning technology, the capability of determining and sharing the positions of object, and in particular one's self-position spawned a myriad of other applications and services, such as Surveying and Mapping, Location Based Services (LBS) and advertisement, Social Network applications, people and vehicle tracking, etc. All this has made positioning technology very popular, and it is installed in all modern mobile devices. Satellite GPS technology is very attractive because the vast majority of GPS receivers are relatively simple and low cost, and the required satellite signal is globally available, without the need for any additional hardware or infrastructure installation. However—it becomes useless in areas where the receivers cannot “see the sky”, or are otherwise deprived of adequate satellite signal. Indoor shopping malls, airport terminals, trade show and exhibition venues, museums—these are just some of the venues where position based applications can be extremely useful, but where GPS technology cannot work, and one has to look for other technologies that can do the task. Existing indoor positioning technologies are mostly based on radio signals, such as WiFi, which also happens to be available in most modern mobile devices. However, these technologies lack adequate precision, or require costly hardware infrastructure installation and maintenance throughout the area where positioning is desired.
3.34375
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The most widespread medium for distributing motion pictures is the videocassette. Because of the different television industry standards used throughout the world, there are an equal number of videocassette standards. An NTSC videotape sold in the United States, for example, will not play on most videocassette players to be found in England. To a far lesser extent, motion pictures are also distributed on optical disk media. These media are for the most part analog recordings, and once again media designed to play on players of one type are incompatible with players of another. Further complicating the need to publish a given motion picture in multiple standards is the fact that there are often two versions of the same motion picture. Typically, the versions may be what are termed R-rated and PG-rated, the former, because of its violence or sexual content, being suitable primarily for adults. Motion picture companies will often produce two different versions of the same film. For example, adult-rated films are generally not shown on airplanes. There are many consumers who will not purchase an adult-rated motion picture, especially if it will be viewed by children in the household. The multiple-standards problem is compounded by the fact that a motion picture may have to be released in two versions, and each of those versions will in turn have to be distributed in multiple standards. Digitally encoded optical disks are in theory far superior for the distribution of motion pictures and other forms of presentation. Especially advantageous is the use of "compressed video," by which it is possible to digitally encode a motion picture on a disk no larger than the present-day audio CD. Especially in the case of compressed video, where there is no real-time analog video signal on a disk, it should be possible to play the same disk throughout the world--the players in any given territory will generate an analog signal of the appropriate standard from the same digitally encoded video source information. It would be highly desirable if the same disk could store two versions of the same motion picture; such a "universal" disk would obviate the need for releasing a motion picture in multiple disk forms. It is therefore an object of this invention to provide a system and method in which multiple versions of the same motion picture are stored on the same software carrier, without requiring multiple full video tracks each devoted to one of the versions. It is another object of this invention to provide a system and method for representing information pertaining to the versions available on the disk, and a player for controlling which version is played. It must be understood that the principles of the present invention are not limited to any particular types of carriers or any particular kinds of software. It is true that the most widespread use foreseen for the invention is by the motion picture industry, and the storage of R-rated and PG-rated versions of the same motion picture on a single disk. However, the invention is not limited to the provision of just two versions on the carrier: the principles of the invention are equally applicable to three or more versions of the same program material. (A practical application of this would be the provision of multiple versions of a tutorial on a single disk, with each version being geared for a different level of expertise.) Not only is the invention not limited to a particular number of versions, but it is not limited to a particular medium--for example, it is applicable to tape carriers and all digital storage media. Thus it is to be understood that the term "software publisher" embraces much more than a motion picture company, and the term "carrier" embraces much more than a digitally encoded optical disk.
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Q: Palindromize this string! Your task is to palindromize a string as follows: Take the string. abcde Reverse it. edcba Remove the first letter. dcba Glue it onto the original string. abcdedcba But here's the catch: since this challenge is about palindromes, your code itself also has to be a palindrome. Remember, this is code-golf, so the code with the smallest number of bytes wins. A: 05AB1E, 1 byte û Try it online! A: Python 3, 41 bytes lambda t:t+t[-2::-1]#]1-::2-[t+t:t adbmal Try it here. A: Dip, 1 byte B Body must be at least 30 characters; you entered 13.
3.125
3
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1. Field of the Invention This invention relates to a bullet loader, more particularly, to a device for reloading bullets into the magazine or clip of a firearm. 2. Prior Art Many small arms, including both rifles and hand guns are provided with magazines or clips in which the bullets are stored for immediate use. In these firearms, ammunition is placed into an elongated, generally rectangular, container, known as a magazine or clip, which is then fitted into a portion of the firearm approximate to the firing chamber; in the case of a pistol, this clip or magazine can be inserted into the handle of the gun. The magazine or clip is closed on five (5) sides of the rectangular shape and open on one rectangular shaped end. Such magazines or clips are spring loaded and are further provided with retaining members over the open end. Ammunition can be placed into the open end of the magazine, piece by piece, and each piece slips past the retaining members to be held until used. As the magazine is being loaded, each succeeding round of ammunition compresses the spring further and each bullet becomes harder to insert. When a magazine is fully loaded, it is fitted into a position adjacent to or against the firing chamber of the weapon. Normally, a bolt it used to extract a round and force it into the firing chamber. As each round is fired, the bolt is forced back, picks up the next round and forces the next round into the firing chamber. The force of the spring pushes each round up into its position in the magazine where the bolt can push it into the firing chamber. The use of a magazine in a firearm provides the convenience of holding a large number of bullets in position for loading in successive order into the firing chamber, thereby allowing for rapid fire of some or all of the loaded bullets. Once the loaded bullets are expended, however, the empty magazine can be quickly removed and a new fully loaded magazine can be quickly inserted into the firearm to resume firing. Thus, the use of magazines is a convenient and effective method of feeding bullets, in rapid succession, into a weapon's firing chamber. On the other hand, reloading bullets into the spent magazine is known to be problematic. More particularly, the structural design of the magazine requires each bullet to be individually loaded through the top ejection end of the magazine past the retainers and downwardly against the force of the compression spring in order to receive the bullet within the magazine. As each bullet is loaded, in sequence, the compression spring in the magazine becomes progressively compressed until the magazine is fully loaded with bullets. Naturally, the resistance of the compression spring against the downward force of loading the bullets into the magazine becomes greater with each successive bullet loaded into the magazine. For many years, bullets have been loaded into empty magazines of firearms by hand, using the fingers to force each bullet downwardly against the force of the compression spring and into captured arrangement within the magazine. This process is time consuming, and quite often frustrating, particularly when the resistance of the compression spring begins to increase. This is particularly true on cold days when a person's fingers are numb, or are enclosed in a glove or mitten, or in a situation such as (military combat) when speed of reloading may be of the essence. A number of devices exist which are adapted to assist the marksman in accomplishing this reloading task. In particular, U.S. Pat. No. 4,464,855 issued to Musgrave on Aug. 14, 1984 teaches a device somewhat useful in solving the above described problem. It teaches a slidably attached apparatus which is provided with a pulling handle and a protrusion which is adapted to push a round of ammunition down into the magazine for insertion of the next round. After each successive round of ammunition is loaded into the magazine, the apparatus must be removed from the magazine and reinserted for the next round. While it does facilitate in solving the problem of reloading, the requirement of removal and reinsertion makes its use somewhat tedious. U.S. Pat. No. 4,689,909 issued to Howard on Sep. 1, 1987, teaches a device which can be fitted over an ammunition magazine. It is adapted with a spring loaded plunger which, when the device is fitted over the magazine and somehow held in place, is used to push the uppermost round down into the magazine to facilitate sliding in the next round. Then the plunger, which is spring loaded, is depressed and the cartridge is fitted all the way into the back of the magazine. Howard is also somewhat helpful, but difficulties may be encountered in holding the device in place against the magazine.
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Q: Java byte type is weird? Could someone explain the java byte type? This doesn't compile: byte b1 = 9; byte b2 = 1; byte b3 = b1 + b2; While this does: byte b4 = 9 + 1; byte b5 = (char)(9+1); In addition, assignment to a long doesn't work, even if the value fits into a byte: byte b7 = (long)127; It gets even weirder with wrappers This compiles: Byte b6 = (int)3; But this doesn't: Integer i = (byte)3; A: Java Language Specification 5.6.2 Binary Numeric Promotion: "Otherwise, both operands are converted type int". So Java converts both operands to and int, so the result of the addition is an int. Addition: The difference between b3 and b4 is, that in b4 it's an Constant Expression (15.28), in b3 it's literal. A: b6 does work due to compile-time narrowing of literal constants. b7 does not work because compile-time narrowing is limited to all primitives but long (kind of strange, no idea why) The interesting part is §5.2 of the JLS: In addition, if the expression is a constant expression (§15.28) of type byte, short, char or int : A narrowing primitive conversion may be used if the type of the variable is byte, short, or char, and the value of the constant expression is representable in the type of the variable. A narrowing primitive conversion followed by a boxing conversion may be used if the type of the variable is : - Byte and the value of the constant expression is representable in the type byte. - Short and the value of the constant expression is representable in the type short. - Character and the value of the constant expression is representable in the type char. If the type of the expression cannot be converted to the type of the variable by a conversion permitted in an assignment context, then a compile-time error occurs. No idea why i does not work though - widening should work just fine and in fact, the compiler should generate something like Integer.valueOf((byte)3); anyhow. Using the explicit call works as expected, i.e. widening is happening. Interestingly enough using the eclipse Java compiler Integer i = (byte) 3; compiles just fine, which leads me to believe you just found a bug in javac - congratulations! (well either that or a bug in the eclipse compiler; but eclipse's behavior seems the correct one to me). FWIW I've reported the bug against javac to oracle.. Finding the right part in the JLS was less work than formatting this that it's somewhat readable - so probably easier if you follow the link instead.
3.046875
3
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The present invention relates to a method for predicting remaining charge of a battery, such as a rechargeable battery of a portable electronic device. In general, chargeable lithium ion batteries are widely used for portable electronic devices, such as notebook personal computers. The lithium ion batteries have advantages such that the operational cost of portable electronic devices can be reduced and the capacity of the current which is instantaneously dischargeable is large. Normally, a machine which has a rechargeable battery so called secondary battery, such as a lithium ion battery, installed therein incorporates a charging circuit which is to be connected to an external power supply to charge the rechargeable battery. To meet the demands for higher performance and size reduction, recent portable devices require a compact charging circuit which can quickly charge a rechargeable battery to a full level. General portable electronic devices include a capability for predicting the remaining charge of a rechargeable battery, when they are in use, in order to avoid problems with data loss by notifying users of the consumption states of the batteries. The prediction of the remaining battery charge should be carried out accurately. As shown in FIG. 1, an ordinary portable electronic device 101, such as a notebook personal computer (PC); is connected to a battery pack 102 which has a plurality of built-in rechargeable batteries (e.g., lithium ion batteries) 102a and 102b and operates on power from each rechargeable battery 102a or 102b. The portable device 101 is also operable on power which is supplied from an external power supply such as an AC adapter 103. A power supply unit for the portable device 101 will be discussed below. The portable device 101 includes a power-supply microcomputer 104, a charger 105, a selection circuit 108, first and second DC—DC converters 109 and 110 and a Low Drop Out regulator (LDO) 111 as a switching regulator. The charger 105, which is connected to the battery pack 102 and the AC adapter 103, supplies a charge voltage and charge current to the rechargeable batteries 102a and 102b in accordance with a control signal from the power-supply microcomputer 104 to charge the rechargeable batteries 102a and 102b with a constant voltage and a constant current. The selection circuit 108 selects at least one of the battery pack 102 (rechargeable batteries 102a and 102b) and the AC adapter 103. The input voltage from the selected power supply is supplied to the first and second DC—DC converters 109 and 110 and the LDO 111. The first DC—DC converter 109 generates a supply voltage to be supplied to a CPU (not shown) from the input voltage. The second DC—DC converter 110 generates a supply voltage to be supplied to peripheral circuits (not shown) from the input voltage. The LDO 111 generates a supply voltage for generating a clock signal (not shown) from the input voltage. The portable device 101 has a remaining-charge predicting capability for predicting the remaining charge of the battery and notifying a user of the predicted remaining charge. The remaining-charge predicting capability will be discussed below. Generally speaking, lithium ion batteries are susceptible to overdischarging. If a user erroneously overdischarges a lithium ion battery, therefore, the performance of the lithium ion battery may not be recovered if it is charged. To prevent such overdischarging, the battery pack 102 incorporates a protection circuit 112 which detects when the voltage of one of the rechargeable batteries 102a and 102b drops below a specified voltage and stops further discharging. When the protection circuit 112 functions, the supply of the power from the rechargeable battery 102a or 102b to the portable device 101 is stopped and the portable device 101 stops operating. At this time, the portable device 101 such as a notebook PC, may suffer loss of data which is being processed. To avoid such a problem, the portable device 101 predicts the remaining charge of each of the rechargeable battery 102a and 102b and notifies the user of the consumption state of the rechargeable battery. The prediction of the remaining battery charge is executed in consideration of various characteristics of the rechargeable batteries 102a and 102b (lithium ion batteries) incorporated in the battery pack 102. The following will explain the characteristics of an ordinary lithium ion battery. FIG. 2A shows a change in discharge characteristic caused by an increase in the number of times a battery set (rechargeable battery) comprising three cells is used (the number of charges/discharges which will be hereinafter called “cycle number”). The vertical scale shows the discharge voltage and the horizontal scale shows the discharge time. A curve A indicates the discharge characteristic with the cycle number being 1 (initial state), and curves B, C and D respectively indicate the discharge characteristics with the cycle number being about 250, about 400 and about 500. A curve E shows the discharge characteristic with the cycle number being about 650. It is apparent from FIG. 2A that as the cycle number increases, the dischargeable capacity of the rechargeable battery decreases, so that the discharge time (usable time) becomes shorter. This phenomenon is called the “cycle degradation characteristic”. In FIG. 2B, the horizontal scale of FIG. 2A has been normalized. The horizontal scale indicates the discharge capacity and shows the end time at 100% discharge. FIG. 2B shows that the rate of voltage reduction of the rechargeable battery is nearly constant irrespective of the cycle number. The cycle life characteristic of the rechargeable battery will be discussed below. FIG. 3 shows the relationship between the cycle number and the discharge capacity which have been measured for three kinds of rechargeable batteries. The discharge capacity of the rechargeable battery decreases as the cycle number increases. For example, a curve F indicates that the discharge capacity when the cycle number is 600 (the capacity at the time of full charge) has dropped to about 30 to 40% of the maximum capacity. The following will discuss the degradation characteristic of the rechargeable battery which varies according to the environment of use. A curve H in FIG. 4 shows the characteristic of the rechargeable battery that has been left out for one month at 45° C., and a curve G shows the characteristic of the rechargeable battery before it has been subjected to the foregoing treatment. The discharge time (use time) of the rechargeable battery varies also depending on the temperature at which it has been used. FIG. 5 is an explanatory diagram showing the relationship between the discharge power and dischargeable capacity at different temperatures of use for two kinds of rechargeable batteries. Curves I to K respectively show the characteristics when one type of rechargeable battery is used at 5° C., 25° C. and 45° C. Curves L to N respectively show the characteristics when the other rechargeable battery is used at 5° C., 25° C. and 45° C. The rechargeable battery that is indicated by the curve I for use temperature of 5° C. can be used for about 2.8 hours with a discharge power of 10 W. The rechargeable battery of the same kind that is indicated by the curve K for use temperature of 45° C. can be used for about 3.2 hours with a discharge power of 10 W. The rechargeable battery of the other kind that is indicated by the curve L for use temperature of 5° C. can be used for about 2.8 hours with a discharge power of 10 W. The rechargeable battery of the same kind that is indicated by the curve N for use temperature of 45° C. can be used for about 3.1 hours with a discharge power of 10 W. Apparently, the dischargeable capacity of the rechargeable battery varies depending on the type, the use temperature and the discharge power. The prediction of the remaining charge of a rechargeable battery has been carried out conventionally in consideration of the aforementioned various characteristics. The remaining charge predicting methods include a method for predicting the remaining charge based on, for example, the battery voltage of the rechargeable battery and a method for predicting the remaining charge based on the integrated values of the charge current and discharge current of the rechargeable battery. FIG. 6 is a schematic diagram of a portable device 121 and a battery pack 122 according to a first prior art system that is equipped with a remaining charge predicting function. The portable device 121 is, for example, a notebook PC. The portable device 121 has a built-in battery pack 122 called a smart battery or an intelligent battery. The battery pack 122 includes plural (three) rechargeable batteries 122a to 122c, a protection circuit 123, a discharge control switch 124, a charge control switch 125, a remaining charge meter 126 as a remaining charge predicting device, an electrically erasable and programmable read only memory (EEPROM) 127 and a first sense resistor 128. FIG. 6 shows only a part of the portable device 121 that actually includes a second sense resistor 129, a charger 130 and a microcomputer 131, for example, a keyboard, which is one type of microcomputer. The rechargeable batteries 122a to 122c, each of which is, for example, a lithium ion battery, are connected in series to one another to form a battery set. The positive terminal of the rechargeable battery 122a is connected to the positive terminal, t1, of the battery pack 122 via the discharge control switch 124, the charge control switch 125 and the first sense resistor 128, and the negative terminal of the rechargeable battery 122c is connected to the negative terminal, t2, of the battery pack 122. The discharge control switch 124 and the charge control switch 125 are formed by first and second P channel MOS transistors. The source of the discharge control switch 124 is connected to the positive terminal of the rechargeable battery 122a. The drains of both switches 124 and 125 are connected together. The source of the charge control switch 125 is connected to the positive terminal t1 of the battery pack 122 via the first sense resistor 128. The transistors of both switches 124 and 125 are connected in such a way that the back gates constitute a forward-biased diode with respect to the charge current and the discharge current. The protection circuit 123 includes an overcharge preventing circuit and overdischarge preventing circuit (neither shown). The protection circuit 123 detects the terminal voltages (cell voltages) of the rechargeable batteries 122a to 122c and turns off the discharge control switch 124 to inhibit discharging when at least one of the cell voltages decreases to or below the specified voltage or reaches an overdischarge state. When at least one of the cell voltages rises above the specified voltage or reaches an overcharge state, on the other hand, the protection circuit 123 turns off the charge control switch 125 to inhibit charging. At the time of charging, the charge current is supplied to the rechargeable batteries 122a to 122c via the charge control switch 125 which has been turned on and the discharge control switch 124. The charger 130 of the portable device 121 is connected to an AC adapter 132 connected to an external power supply. The charger 130 controls the charge current based on the value of the current that flows across the second sense resistor 129. At the time of discharging, each of the rechargeable batteries 122a to 122c supplies the discharge current to the portable device 121 via the discharge control switch 124 which has been turned on and the charge control switch 125. The remaining charge meter 126 includes a microcomputer (not shown) which measures the charge current/discharge current that flows across the first sense resistor 128 and predicts the remaining charge based on the integral value of that measured current and each cell voltage detected by the protection circuit 123. The remaining charge meter 126 stores the predicted remaining charge in the EEPROM 127 and supplies the predicted remaining charge to the keyboard microcomputer 131 provided in the portable device 121. When receiving the predicted value for the remaining charge from the remaining charge meter 126, the keyboard microcomputer 131 displays the remaining battery charge on an unillustrated display unit. FIG. 7 shows a second prior art system equipped with a remaining charge predicting function. A portable device 141 is, for example, a notebook PC. The portable device 141 has a built-in battery pack 142. According to the second prior art, the battery pack 142 differs from the battery pack in FIG. 6 in that it has a integrating current meter 143 as a remaining charge predicting device. The integrating current meter 143 measures the charge current/discharge current that flows across the first sense resistor 128 and supplies a current integrated value to a power management microcomputer 144 of the portable device 141. Then, the power management microcomputer 144 calculates a remaining charge predicted value based on the current integrated value output from the integrating current meter 143 and displays the remaining battery charge on an unillustrated display unit based on the predicted value. These prior art systems have the following shortcomings: 1. Shortcoming Pertaining to Prediction of Remaining Charge In the first prior art system shown in FIG. 6, the remaining charge meter 126 calculates a remaining charge predicted value based on the cell voltage of each of the rechargeable batteries 122a to 122c and the integrated values of the charge current and discharge current and supplies the predicted value to the portable device 121. While this ensures highly precise prediction of the remaining charge, the manufacturing cost for the battery pack 122 increases due to the microcomputer provided in the remaining charge meter 126. This makes the battery pack 122 expensive. In the second prior art system shown in FIG. 7, on the other hand, because the battery pack 142 is not equipped with a microcomputer, an increase in the manufacturing cost for the battery pack 142 is nit incurred. However, in the battery pack 142, the integrating current meter 143 predicts the remaining charge of the rechargeable battery only by detecting the current value. As shown in FIG. 3, when the cycle number of the rechargeable battery increases, the discharge capacity decreases, so that mere prediction of the remaining charge based on current integration would result in inaccurate prediction of the remaining charge. In a case where the battery pack 142 incorporates plural rechargeable batteries 122a to 122c, particularly, their capacities (terminal voltages) vary, thus lowering the precision of the prediction of the remaining charge. 2. Charge-Oriented Shortcoming In the first prior art system, the charger 130 detects the charge current that flows across the second sense resistor 129 and charges the rechargeable batteries 122a to 122c with the constant voltage and constant current based on the detection result. To precisely perform such charging with the constant voltage and constant current, it is necessary to improve the precision of the current detection done by the charger 130. In this respect, normally, a sense resistor of a high precision type is used as the second sense resistor 129 that is provided to detect the current. This disadvantageously increases the manufacturing cost for the charger 130. Further, such a high precision type resistor is large in size, which undesirably enlarges the charger 130. This shortcoming also arises in the second prior art system.
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Natural colorants: Pigment stability and extraction yield enhancement via utilization of appropriate pretreatment and extraction methods. Natural colorants from plant-based materials have gained increasing popularity due to health consciousness of consumers. Among the many steps involved in the production of natural colorants, pigment extraction is one of the most important. Soxhlet extraction, maceration, and hydrodistillation are conventional methods that have been widely used in industry and laboratory for such a purpose. Recently, various non-conventional methods, such as supercritical fluid extraction, pressurized liquid extraction, microwave-assisted extraction, ultrasound-assisted extraction, pulsed-electric field extraction, and enzyme-assisted extraction have emerged as alternatives to conventional methods due to the advantages of the former in terms of smaller solvent consumption, shorter extraction time, and more environment-friendliness. Prior to the extraction step, pretreatment of plant materials to enhance the stability of natural pigments is another important step that must be carefully taken care of. In this paper, a comprehensive review of appropriate pretreatment and extraction methods for chlorophylls, carotenoids, betalains, and anthocyanins, which are major classes of plant pigments, is provided by using pigment stability and extraction yield as assessment criteria.
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Silicon-on-insulator (SOI) wafer is a starting material for making advanced semiconductor chips. Currently the most advanced method of making the SOI wafers is a layer transfer method. In the layer transfer method, a thin film of crystalline material is delaminated from a first wafer and laminated on a surface of a second wafer. The first wafer is called a donor wafer, and the second one is called a destination wafer. Either the donor or the destination wafer or both can have insulating films on their surfaces. Those insulator films further appear as a middle layer in a 3-layer sandwich structure that is obtained by the layer transfer process. The sandwich structure which consists of a silicon wafer with silicon dioxide and silicon films on its top is referred as the SOI wafer, and it is mostly used in mass production of advanced chips. The layer transfer process was invented by Bruel, and described in U.S. Pat. No. 5,374,564 awarded to him. Bruel's process was later named Smart-Cut. The Smart-Cut process sequence is schematically illustrated on FIG. 1 and FIG. 2. Due to the Smart-Cut process, FIG. 1A an initial donor wafer 101 with a silicon dioxide layer 102 is provided. Then, FIG. 1B, the wafer 101 is implanted through oxide 102 with hydrogen ions 103 which stops inside of silicon wafer and form a hydrogen-rich layer 104. The layer 104 divides the wafer 101 into silicon film 105 to be further transferred and a leftover part 106. Then, FIG. 1C the donor wafer 101 is brought into contact with a destination wafer 107 and a prebonded wafer assembly 108 with bonding interface 109 is formed. Then, FIG. 1D the assembly 108 is heated to cause a spontaneous cleavage along the hydrogen-rich layer 104 and make a SOI wafer 109 and a leftover wafer 110. The SOI wafer 109 consists of a silicon wafer 107 covered with a silicon dioxide film 111 and a single crystalline silicon film 112 having a work side surface 113. More processing details 201–208 of the Smart-Cut are illustrated by FIG. 2. The Smart-Cut process still has drawbacks that where partially eliminated by numerical improvements as described in patents awarded to Goesele—U.S. Pat. No. 6,150,239, to Henley—U.S. Pat. No. 5,994,207, to Usenko—U.S. Pat. No. 6,352,909, and in others. The most important drawbacks of the Smart-Cut are as follows: (1) difficult to get thin transferred layer; (2) high manufacturing cost. The difficulty in the transfer of thinner layers in the Smart-Cut is caused by the use of hydrogen implantation into plain silicon lattice. In the Smart-Cut, hydrogen implantation depth defines a plane along which a film is further delaminated from the donor wafer. Hydrogen is the lightest ion; therefore it penetrates into targets deeper than any other ion being implanted. At typical hydrogen ion energy of about 100 keV used in the Smart-Cut process, the hydrogen penetrates to a depth of about 1 micrometer below the silicon surface. And, about 1-micron thick layer is delaminated from a donor substrate and laminated to a destination substrate. The typical final Unibond™ wafer (SOI wafer obtained by Smart-Cut process) therefore has about 1-micron thick superficial silicon, or about 1-micron thick stacks consisting of the superficial silicon, and an insulative film. Chip manufacturing, however, requires much thinner superficial silicon, and insulator layer thicknesses. Manufacturing of mainstream chips that have fully depleted CMOS architecture requires the thickness to be no more than 50 nanometers. In the future, manufacturing chips will require even thinner silicon layers as the chipmaking advances mainly by scaling down all features, including the lateral and vertical dimensions of transistors constituting the chips. Smart-cut however, is limited to layer transfers in excess of 200 nm. There were attempts to obtain thinner layers by the Smart-Cut by lowering of hydrogen implantation energy. Bruel's patent does not claim hydrogen energy range, but later it was found that the lowest energy is about 20 keV [Y. V. Nastaushev, T. Gavrilova, M. Kachanova, L. Nenasheva, V. Kolosanov, O. V. Naumova, V. P. Popov, A. L. Aseev “20-nm Resolution of electron lithography for the nano-devices on ultrathin SOI film” Materials Science and Engineering C vol. 19 (2002) 189–192]. At lower energies, Smart-Cut process fails. In the case of low implantation energy, implanted hydrogen does not form an in-depth distribution with a clear peak at some depth. Instead, hydrogen is distributed quite evenly from surface to some depth in silicon. When there is no a well defined peak, the donor wafer is either not cleavable, or it cleaves at various depths along the wafer area, and a layer that is highly non-uniform in thickness is further delaminated and transferred onto a destination wafer. The relative widening of the peak of the implanted specie with energy decrease is a general feature of ion implantation that relates to all kinds of implanted ions. At higher energies, ions show an average depth where they stop (called projection range) that is much bigger, than average depth deviation (called struggle). At low energies, the struggle is approaching ½ of the projection range, and therefore the ion distribution looses peak pattern with energy lowering. High energy (tens of keV or more) ions predominantly loose their energy while penetrating a target by transferring energy to electrons of the target. When ion energy drops to about 20 keV, another mechanism of interaction with a target becomes dominant. The mechanism is displacing of target atoms. Therefore at the end of its track, ion makes numerical displacements of target lattice atoms and quickly stops. This results in quite narrow peak of distribution of high energy ions. Implanting of sub-20-keV ions predominantly results in displacing of target lattice atoms beginning from initial hit into the lattice; in other words, the low energy ion begins to destroy target lattice as soon as it hits the crystal surface. Therefore sub-20-keV implanting results in in-depth profile of implanted ions that is rather diffused, then a peak-like. The diffused profile causes the Smart-Cur failure. Another reason why Smart-Cut fails to transfer thin films relates to surface damage by sub-20 keV ions. The damaged surface has higher roughness then an initial polished surface. Rough surface donor cannot be bonded to the destination wafer. Without bonding, the layer cannot be transferred, and Smart-Cut fails. Another cause why Smart-Cut fails to transfer thin films is a premature blistering of wafer surface if the wafer is implanted with low energy ions. Hydrogen implantation results in creating of pressurized hydrogen bubbles under wafer surface. Low energy implantation results in shallow location of the bubbles. Thinner layer of silicon covering the bubbles is easier to break. The wafers implanted with sub-20 keV hydrogen ions blister at implantation doses that are lower than a dose needed for layer transfer. Attempts to obtain thin superficial silicon by transferring of 200-nm Si—SiO2 stacks mostly consisting from SiO2 (like 50 nm of Si and 150 nm of SiO2) also fails. In this case implanted hydrogen segregates at Si—SiO2 interface instead of forming a cleavage plane inside of silicon. Only SiO2 layer transfers are obtained, and SOI wafers are not obtained. Additional thinning of transferred films by polishing or etching is typically used to extend the Smart-Cut capabilities into sub-100 nm range. Thinning however increases thickness non-uniformity of the superficial crystalline film of SOI wafer that is highly undesirable. High manufacturing costs of the Smart-Cut are caused by necessity of prolonged hydrogen implanting. Smart-Cut requires implanting of hydrogen in a dose exceeding 4×1016 cm−2. Even though this dose is two orders of magnitude bigger, than doses used in chip manufacturing, modern implanters allow getting reasonably high throughput for this dose as they have high ion beam current. Hydrogen implantation in Smart-Cut cannot however benefit from high ion beam current. The higher the beam current, the stronger is target heating. If the target (i.e, silicon wafer) is heated over about 80° C. during the implantation, Smart-Cut fails. Heating of the wafer under implantation causes premature blistering. Due to its low solubility in silicon, implanted hydrogen immediately segregates into pressurized bubbles. At elevated temperature the bubbles develop high pressure and cause fracture of silicon film covering the bubble. FIG. 3 shows a typical picture of wafer that is implanted at high beam current. On FIG. 3, areas 301 are not blistered, while areas 302 are blistered. In this case, the blistered areas are closer to the wafer center which had worse contact to a thermal sink and was heated to higher temperature. To obtain higher throughput of Smart-Cut implantation, cooling of the silicon wafer during the Smart-Cut implantation is typically used. The cooling, however, allows increasing the hydrogen ion beam current no more then by a factor of 2 or 3. It means that the implantation time for one wafer can be decreased from several hours per wafer to about one hour per wafer that is very low throughput in wafer production. Batch implanters process up to about a dozen wafers simultaneously. Those implanters allow increasing the throughput by about a factor equal to a number of the simultaneously processed wafers. Therefore the best achievable throughput in the Smart-Cut is limited to about 10 wph (wafers per hour). This is not enough to achieve a cost-efficient SOI wafer production. To obtain higher throughput of Smart-Cut implantation, plasma immersion ion implantation was suggested. Henley in U.S. Pat. No. 6,582,999 as well as in his previous 20 related patents (U.S. Pat. Nos. 6,548,382, 6,528,391, 6,511,899, 6,458,672, 6,413,837, 6,321,134, 6,291,326, 6,291,314, 6,290,804, 6,248,649, 6,207,005, 6,162,705, 6,155,909, 6,153,524, 6,146,979, 6,083,324, 6,013,563, 6,010,579, 5,994,207, 5,985,742) describes using of plasma immersion ion implantation instead of conventional beam implantation to introduce hydrogen into silicon to a defined plane for further cleavage and SOI wafer production. The plasma immersion ion implantation is similar to the regular implantation in many considerations. The plasma immersion equipment can be described as a simplified ion implanter: a regular implanter but not equipped with ion separator. Another important feature of the plasma immersion ion implantation is that it is pulsed. In a wafer being implanted, all vacancies and interstitials are generated during the pulse, and therefore, it results in denser concentration of vacancies, and interstitials at the end of the pulse as compared to the steady state defect generation. The denser concentration of the generated defects causes more efficient annihilation of the defects. Finally, in the Smart-Cut at room temperature, about 50% of hydrogen find a vacancy, form a hydrogen-vacancy site, and retain in the silicon, while less then 10% of hydrogen introduces by plasma immersion ion implantation find a vacancy and retain in silicon. However, the plasma immersion ion implantation has an advantage over the beam implantation as it allows obtaining much higher hydrogen fluences. The beam implantation is limited to no more then about 0.1 A hydrogen ion beam current, while plasma immersion ion implantation can yield up to 10 A in averaged hydrogen current into the wafer. Therefore, the plasma immersion ion implantation can potentially give better wafer throughput, than the beam implantation, even though the hydrogen losses are much higher in the plasma immersion case. The direct replacement of the beam implantation by plasma immersion in the Smart-Cut results, however, in much worse quality of final SOI wafers. The reason is that in the plasma immersion case, hydrogen having energies from almost zero to about 40 keV is implanted. That results in hydrogen retention in wide layer from surface to about 0.5 micrometer. Immediately after implantation, hydrogen is in form of bubbles in silicon. High temperature anneal after cleavage removes hydrogen from silicon leaving empty voids in place of hydrogen bubbles. A crystalline quality of that heavily hydrogenated silicon cannot be healed by annealing to a level required by chip production. Henley does not describe in his patents, what is the minimum hydrogen dose needed to enable the layer transfer with plasma immersion ion implantation. The minimum dose was experimentally determined independently, and it exceeds 1018 cm−2, i.e., much higher dose than in the Smart-Cut. Silicon has about 1018 cm−3 contamination of oxygen, and also non-negligible concentration of other doping and unintentional impurities evenly distributed in silicon. Some of them works as infinite traps for hydrogen; and the higher dose hydrogen implantation, the bigger amount of hydrogen platelets and bubbles will be created on these unintentional and unavoidable traps. The hydrogen platelets and the bubbles are non-point defects, and silicon that contains these features cannot be annealed to restore its initial perfect lattice. Finally, plasma immersion implantation version of the Smart-Cut results in SOI wafers with low quality superficial silicon. That silicon contains voids in high density. Another problem with Henley's process is that it results in thinner transferred layers at wafer periphery as compared to the wafer center. This is because the plasma immersion implantation equipment is characterized in non-uniform hydrogen energy across the wafer; higher energy at the center, and lower energy near the edges. Fan et al. in Z. Fan, P. K. Chu, N. W. Cheung, C. Chan, Thickness uniformity of silicon-on-insulator fabricated by plasma immersion ion implantation and ion cut, IEEE Transactions on Plasma Science, Vol. 27, 1999, pages 633–636 given an experimental evidence of thickness non-uniformity of the plasma immersion implantation version of the Smart-Cut; the thickness non-uniformity is a serious quality problem in the final SOI wafer. As it is explained above, the Smart-Cut can be characterized as a trap-controlled process. An availability of properly located traps determines the Smart-Cut efficacy. Without the traps, hydrogen does not retain in silicon, it outdiffuses. In previous art, attempts where made to improve the Smart-Cut throughput by pre-forming a trap layer for hydrogen and further hydrogen injection. Agarwal et al. described helium-than-hydrogen implantation; Goesele at al., Bower, and Nastasi et al. described boron-than-hydrogen implantation; Usenko described trap-creating implantation followed by hydrogenation by either electrolytic or plasma means. These Smart-Cut improvements either partially resolve the thickness and cost related Smart-Cut issues, or create quality issues. Agarwal et al (A. Agarwal, T. E. Haynes, V. C. Venezia, O. W. Holland, and D. J. Eaglesham, “Efficient production of silicon-on-insulator films by co-implantation of He+ with H+”, Applied Physics Letters, vol. 72 (1998), pp. 1086–1088) describe dual implantation to achieve layer transfer at lower total implantation dose. They report they got the layer transfer at a combined dose of their sequential helium-then-hydrogen implants that is about 2 times lower then minimum dose required in the Smart-Cut (7.5×1015+1×1016 cm−2 against 4×1016 cm −2). Due to Agarwal, helium and hydrogen implantation depths should be the same. Even though, they do not attribute the lower total dose needed to the trapping phenomena, this is a possible explanation in the lowering of minimum required dose they observe. Agarwal's approach, however, does not solve the thickness problems of the Smart-Cut. Goesele et al. in U.S. Pat. No. 6,150,239 described boron-than-hydrogen implantation to achieve a cleavage at lower total implantation dose. They also report about 2-fold drop in minimum implantation dose required to enable the layer transfer. However, Goesele suggests implantation in conditions when boron implantation peak coincide with hydrogen implantation peak. That restrict hydrogen implantation conditions in peakless, i.e., low energy mode. Subsequently, the thickness limitation is the same as in the Smart-Cut, and thin transfers are not enabled by Goesele. Also, Goesele does not describe that the post-boron hydrogen implantation can be performed in high beam current mode. Therefore the throughput problem is not solved by Goesele either. Bower in U.S. Pat. No. 6,812,547 describes layer transfer where he implants boron, then anneal the wafer, then implant hydrogen to form a fragile layer for further cleavage at a plane where boron acceptor centers are located. Due to Bower's teaching, the boron and hydrogen energies are not required to be chosen by condition that they have the same projection range. Hydrogen can be implanted anywhere in the wafer, and then hydrogen diffuses until it finds boron acceptor centers, and then hydrogen gets trapped at these centers. Therefore, potentially the Bower's technique might be free from limitation on thickness of layer transfers that is inherent to the Smart-Cut, to Agarwal's, and to Goesele's processes, and it might enable ultrathin layer transfers. Even though Bower describes 330-nm transfer only, let us analyze that possibility. We believe that Bower's process cannot enable the ultrathin transfers. The reasons are as follows. Bower teaches to introduce acceptor centers into silicon to enable the film delamination. Due to Bower's teaching, annealing of the boron-implanted wafer result in complete removal of implantation damages and in electrical activation of boron. The activated boron creates acceptor centers in silicon that further work as traps for hydrogen. Hydrogen is implanted deeper into silicon and diffuse after the implantation until it reaches the boron traps. The acceptor impurity (boron) is introduced in an amount of 1015 cm−2 and activated by annealing at 950° C. due to Bower. An acceptor center concentration in semiconductor cannot exceed a solubility limit of given acceptor impurity in semiconductor at activation temperature. In Bower's case, boron solubility limit at 950° C. is 2×1020/cm3. Therefore, a layer of (1015 cm−2)/(2×1020/cm3)=50 nm in thickness will be doped to the boron solubility limit. This means, that a layer with a thickness of 50 nm will trap hydrogen, and it further means that the splitting plane is defined with 50-nm accuracy. The wafer will split anywhere inside of the 50 nm band. Then, at the best, the as-cleaved surface will have a roughness of 50 nm. This says that sub-100-nm layer transfers will be extremely non-uniform in thickness, and thus are not technically featurable for thin SOI production. Another reason, why Bower's teaching cannot be applied for manufacturing of thin SOI relates to unwanted altering of electrical properties of the transferred silicon layer. Silicon, doped with boron to 2×1020/cm3 has resistivity of 5×10−4 Ωcm. Chips cannot be manufactured in these heavy doped films for several reasons, for example, because carrier mobility drastically drops in heavy doped semiconductors, and also because a depleted zone will not extend through entire thickness of silicon film, so fully depleted devices cannot be manufactured. Nastasi et al. in J. K. Lee, T. Hochbauer, R. D. Averitt, and M. Nastasi, “Role of Boron for Defect Evolution in Hydrogen-Implanted Silicon”, Applied Physics Letters, vol. 83, (2003), pp. 3042–3044 describe that at some combination of boron-then-hydrogen implantation conditions they observe that hydrogen follow either boron-caused damage peak, or boron peak, but they did not found conditions that allow very thin layer transfer. Usenko in U.S. Pat. No. 6,352,909 describes a process for fabricating SOI wafers using ultrathin transfer of silicon film from a donor wafer to a destination wafer. Usenko uses silicon-into-silicon or other electrically non-active implants to form a shallow trap layer for hydrogen in silicon, and further insertion of atomic hydrogen into the wafer either by electrolytic means or from hydrogen plasma. This process is free from limitations inherent to Smart-Cut cut process as relative to thickness and to implant-related cost, but it is more difficult to get high quality SOI wafers using the U.S. Pat. No. 6,352,909 process. The quality problems appear in both, electrolytic, and plasma methods of hydrogenation. If hydrogen plasma contains low-energy hydrogen (as it happen, for example, in RF plasma), the low-energy hydrogen preferentially interact with silicon surface, instead of entering into the silicon lattice and diffusing to a trap layer. The interaction with surface results in silicon etching. The etching preferentially proceeds on defected surface areas, therefore the etching is not area-uniform, and roughness of silicon wafer surface increases. The rough surface wafer is difficult to bond to a destination wafer. The roughness causes bonding voids between the wafers. The voids cause layer transfer faults, and a final SOI wafer has areas with missing superficial silicon. These wafers are rejected and are not useful anymore. In a case of electrolytic hydrogenation, the chemical solution used as an electrolyte also etches silicon surface. The etching is the strongest in areas where silicon crystalline microdefects intersect the wafer surface. Etching pits appear in these areas. Further, the pits translate into voids of transferred silicon film, and the SOI wafers with missing superficial silicon areas are rejected again. It will be beneficial to the art to have a process that combines high quality of final SOI wafers as in Smart-Cut process and ability of fabricating ultrathin SOI with high throughput as in processes that use trapping of hydrogen.
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Sports involving spherical game balls, such as basketball, soccer, and volleyball, are enjoyed by millions of spectators and players around the world. An important characteristic of these game balls is how visible the ball is to a spectator or a player. The games are played in a wide variety of lighting conditions. For example, games are played outdoors, indoors, under artificial light, under natural light, in bright sunlight, and at twilight. Ball visibility is affected by the color or colors used on the ball, yet in most game balls the color(s) is chosen based on aesthetics or tradition. Some attempts have been made to produce high-visibility balls using bright, fluorescent colors. Another approach has been to provide a light source within the ball, for example, an LED. Yet another approach uses phosphorescent pigments which absorb and then re-emit light. However, these approaches are relatively expensive. Thus, a heretofore unaddressed need exists in the industry to address the aforementioned deficiencies and inadequacies.
3.3125
3
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Staying celibate can be a difficult task, but bdelloid rotifers have managed to survive without sex for nearly 50 million years. Scientists now think they have cracked the secret to these microscopic animals’ success: recombining their own genes in new ways and stealing genes from other organisms living nearby, thus keeping genetic diversity alive and well—even without the DNA from a mate. “This animal has lost its sexuality,” said study co-author Olivier Jaillon of Genoscope, part of the Institut de Génomique du CEA in France. Jaillon said the results of the study gave him one of the very rare moments in a career when you feel you’ve really “found something.” Reproductive Mystery Bdelloid rotifers are microscopic, multicellular animals that look and move a lot like leeches (“bdelloid” is from the Greek for “leech”). They generally live in freshwater, moist soil, and other damp environments. And these unassuming animals have some pretty cool superpowers: They can withstand long periods of being dried out, as well as massive doses of radiation that would kill pretty much every other living thing. Despite these traits, bdelloid rotifers are mainly known in the research world for their 40-million-year-long dry spell in the sack. Although biologists long suspected that these microscopic animals never reproduced sexually—they generally reproduce via an asexual method known as parthenogenesis, in which the offspring is the clone of the parent—the assertion remained controversial for several reasons. One of the key purposes of sexual reproduction is to provide an ongoing source of genetic diversity and not let harmful mutations accumulate. Since these rotifers were such an evolutionary success, scientists found it difficult to believe the animals weren’t reproducing sexually. (Get a genetics overview.) This Female Insect Fakes Her Own Death to Avoid Sex READ: May 2, 2017 - For some animals, sex can be a risky activity, especially if the timing isn’t right. Copulation can be energy-intensive, and can cause injury to one of the partners. One species of dragonfly, called the moorland hawker, native to the Swiss Alps, has evolved an unusual strategy to mitigate possible danger. Females are especially vulnerable right after egg laying, so if they spy a male approaching when they’re leaving a newly deposited clutch, they sometimes play dead. The ploy often works, with the male passing the seeming carcass by, and the female flying away when the male has moved on.READ: Why Female Dragonflies Go to Extreme Lengths to Avoid Sex Although sexual reproduction is extremely beneficial, it’s not without costs: Time spent finding a mate is time not spent finding food or hiding from predators. There’s also no guarantee that the offspring will be as well adapted to the environment as the parents. Yet just because sexual reproduction in bdelloid rotifers had never been observed didn’t mean it never happened. Dr. Ruth of Rotifers To settle this issue, Jaillon, along with Jean-François Flot and Karine Van Doninck, at the University of Namur in Belgium, and colleagues focused their efforts on one particular species of bdelloid rotifer, Adineta vaga. This species is easy to raise in the lab, and previous work had indicated that it had one of the smallest genomes of any of the bdelloid rotifers, which would make it easier for the scientists to sequence. The sequencing results weren’t quite what the researchers had anticipated. “We were all surprised by the genome structure, as nothing like this had been observed before,” said Flot, whose study appeared this week in the journal Nature. The genome of A. vaga had an unusual array of characteristics that, together, made it basically impossible for the rotifer to reproduce sexually. (Also see “Wild Romance: Weird Animal Courtship and Mating Rituals.”) A. vaga has modifications that made its chromosomes—or DNA molecules—nonidentical, which is also unusual in the animal kingdom. This meant that A. vaga‘s sex cells couldn’t complete a key phase of meiosis—or cell division—known as crossing over, in which each chromosome lines up next to its partner and they swap portions of DNA. The genes present on each chromosome have been shuffled across the genome, which means the rotifers’ chromosomes aren’t alike enough to line up for the crossing over. In fact, Van Donink pointed out, the chromosomes of A. vaga had many of the same genetic characteristics of the human Y chromosome, which also does not undergo crossing over. This similarity helps confirm that this step does not happen and these bdelloid rotifers are not capable of sexual reproduction. Mission to Mars? Although A. vaga can’t use crossing over to get rid of harmful mutations, it does use a similar method to shuffle its genes. And, like all bdelloids, A. vaga is a notorious gene thief. Its genome sequence revealed that 8 percent of its genes had come from non-animals like prokaryotes and fungi. This, along with its ability to shuffle genes, will likely keep the rotifer alive and well for at least another 40 million years. “Because of these incredible survival abilities and the fact that, being asexual, a single individual can start a whole population, I wouldn’t be surprised if bdelloid rotifers were able to survive space travel and colonize other planets such as Mars,” Flot said.
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Kwade (Comminution) comminution kinetics - Columbia University than size x are being formed is given in equation (3): Wx = Kxt. (3) where W x comminution operation, such as ball milling, can . kinetics of particle formation in a ball mill. one .. responding daily mill capacities showed a linear relationship,. The Power Consumption Calculation of a Ball Drum Mill - Idosi Mill (grinding)Stone Crusher Machine for Sale A mill is a device that breaks solid materials into smaller pieces by grinding, crushing, or cutting To calculate the needed grinding work against the grain size changing three half-empirical models are . The power predictions for ball mills typically use the following form of the Bond equation: . "Mills and GMDs" ( PDF). Basics in Minerals Processing Handbook as pdf file - Exploring ball size distribution in coal grinding mills (PDF Download Article (PDF Available) in Powder Technology 257:68–73 · May 2014 with 202 Reads new balls are added to the mill, have significant effects on the mill capacity and the milling The effect of the ball size distribution on the milling rate of coal has been .. These equations were incorporated into our simulation so ftware. 1 MODELING THE SPECIFIC GRINDING ENERGY AND BALL-MILL Effect of circulating load and classifiion efficiency on HPGR and pdf. Effect of circulating load and classifiion efficiency on HPGR and ball mill capacity Ball mill capacity tends to increase with larger circulating loads, but this The first order grinding law is described by Equation 1: í dD dt Where: dR dt
3.09375
3
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As fans of the science fiction genre, we’re all aware that science fiction authors frequently try to predict the future of technology and science in a realistic way. In fact, for many readers of science fiction, that’s a big part of the appeal versus fantasy novels or ordinary fiction. This great infographic from Printerinks.com takes a look at what existing technologies and discoveries were first predicted in books. From the two moons of Mars first mentioned in Gulliver’s Travels in 1735, to government spying that was so central to the story of George Orwell’s 1984, and to the real-time translation provided by the Babble fish in The Hitchhiker’s Guide to the Galaxy first published in 1980. To learn more, take a look at It’s Okay to be Smart’s video looking at the predictions of visionary authors like Isaac Asimov and Arthur C. Clarke or AT&T’s timeline of Science Fiction to Reality.
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What You Should Know About Gum Disease and Tooth Decay Webster’s dictionary defines the word”decay” as”an act of departure gradually from an audio or prosperous state to one of less perfection; to be slowly diminished; to deteriorateto become rotten.” Webster defines the word”disease” as”a particular destructive process from the body with a specific cause and effect; an uneasiness; distress; or some other death from the healthy condition.” With all these definitions, we may be able to understand the dentist when she or he informs us that a tooth has decayed and the fascia requires a filling, or the gum has a disorder pocket shaped around the tooth and distance needs a deep cleaning. Unfortunately, these definitions by Webster for the word”decay” along with the word”disease” don’t answer the question as to”why” the tooth and the gum pocket developed in the first place. Maybe this article can help you to understand and answer this query as to why you need treatments in the dental chair. Animal teeth, especially the enamel, covering the outer surfaces of their teeth, are the toughest structures ever to grow in the animal body. It’s Nature’s design and Nature meant the teeth of any animal to last the creature’s lifetime, including lasting the life for us human animals. To observe this natural wellbeing, all you need to do is go any natural history museum. There you’ll find many sorts of animal skeletons, such as a number of those hominid ancestors which are on the same branch of Nature’s family tree with us. You will discover in certain museums complete skeletons of dinosaurs which are 65 million years old. These dinosaur skulls have their teeth without any tooth decay or gum disease, revealing healthy bone, surrounding their healthy teeth. These observations support the contention that the teeth of creatures must last the creature’s lifetime, because without them, how can they live and survive? From skeletonswe could get a fantastic deal of understanding in the lives of creatures that preceded us and even more knowledge when we compare them with the wild creatures of the current day. Animals of all kinds, living in the past as well as those living in the wild now, continue to display the same glorious, disease-free mouths as the ones displayed and seen from the skeletons in our natural history museums. Edmonton Emergency Dentists & Dental Clinic | Emergency Dental Edmonton At archaeological sites all over the world, scientists are finding intact hominid skeletons which are millions of years old. In archeological research, teeth serve an important role like the usage of contemporary fingerprints in criminology. Archaeologists will make use of these teeth when identifying certain species of animals as well as hominids of the prehistoric past. Archeologists will confirm that their tooth enamel would be the most durable biological substance known to science and that teeth are more likely than bones to survive the ravages of evolutionary time. In addition, it has been said that animal teeth are almost indestructible, just witnesses a wild carnivore with their teeth for crushing bones while still eating. These observations of teeth being almost indestructible and decay-free from 65 million-year-old dinosaurs, in millions of year old hominids and other animal skeletons in our natural history museums, in addition to from the wild animals living now, begs another question. Why is it that we modern humans have numerous dental problems with tooth decay and gum disease? The 1 thing all these previous animals and the crazy ones living now have in common, which we have overlooked, is the fact that the past wild animals did not and the current wild animals do not eat foods that are cooked. They only ate and eat from Nature’s food source, which are the seasonal environmental foods of planet Earth. Additionally, not one of those past and present wild animals ever cleaned their teethusing a toothbrush, toothpaste, mouthwash or floss, nevertheless their teeth and gums remained disease-free during their lives. This proof is everywhere throughout evolutionary period in virtually every intact animal skull, revealing all their teeth and surrounding encouraging bone. Emergency Dental Care To understand this natural phenomenon, we need to know more about the healthy balance which exists in all Nature’s animal mouths, which has happened to each evolutionary creature. This natural innate balance entails three physical places. First, we must understand the issues, including the teeth, tongue, gums and other oral soft tissues, the jawbones and jaw joints, neck and head muscles, taste buds and the salivary glands with their alkalizing fluids. Second, we must comprehend the germs that naturally reside in the creature mouth. And next, we need to comprehend the evolutionary planetary foods consumed by the animals of the time. The animal’s five physical senses are also involved and will be the biggest aspect of this balancing picture for all of Nature’s living creatures. These natural senses for living to pay strict attention to sound, sight, touch, smell, and flavor that all the creatures use in the discovery of the foods. The adventures of these senses also turn on many contributing physiological functions that are everywhere in the body. These senses direct and help in the consumption processes of meals, which will continue the animal’s lifestyle. The senses are used for gathering foods to consume, digest, assimilate, package and keep the energy and nutrients from the foods consumed. The energy and nutrients are used for instant or for future use, allowing the cells of an animal body their living adventures.
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Q: Can someone tell me the very basics of how computer programming works? What makes all the words of a programming language actually do anything? I mean, what's actually happening to make the computer know what all of those words mean? If I verbally tell my my computer to do something, it doesn't do it, because it doesn't understand. So how exactly can these human words written into a language actually cause the computer to do some desirable activity? A: It all starts with the CPU or processor. Each processor type has a defined set of instructions it's able to perform. These instructions operate over ones and zeroes, which in turn represent whatever you wish them to: numbers, letters, even the instructions themselves. At the lowest level, a zero is determined by the presence of a certain voltage (usually near 0V) at a transistor and a 1 is the presence of a different voltage (CPU dependent, say 5V) The machine instructions themselves are sets of zeroes and ones placed in a special locations called registers in the processor, the processor takes the instruction and its operands from specific locations and performs the operation, placing the result on yet another location, afterwards going to fetch the next instruction and so on and so forth until it runs out of instructions to perform or is turned off. A simple example. Let's say the machine instruction 001 means add two numbers. Then you write a program that adds two numbers, usually like this: 4 + 5 Then you pass this text to a compiler which will generate the adequate machine code for the processor you will run the program on (sidenote, you can compile code to be run in a different processor from the one you are currently running, it's a process called cross compilation and it's useful, for instance, in embedded platforms). Well, the compiler will end up generating, roughly, 001 00000100 00000101 with additional boilerplate machine code to place the 001 instruction in the next instruction register (instruction pointer) and the binary encoded numbers in data registers (or RAM). The process of generating machine code from structured languages is fairly complex and places limits on how normal these languages can end up looking like. That's why you can't write a program in english, there's too much ambiguity in it for a compiler to be able to generate the proper sequence of zeroes and ones. The instructions CPUs can execute are fairly basic and simple, addition, division, negation, read from RAM, place in RAM, read from register, and so on. The next question is, how can these simple instructions over numbers generate all the wonders we see in computing (internet, games, movie players, etc.)? It basically boils down to the creation of adequate models, for instance a 3D gaming engine has a mathematical model that represents the game world and can calculate the position/collisions of game objects based on it. These models are built on very many of these small instructions, and here's where high level languages (which are not machine code) really shine because they raise the abstraction level and you can then think closer to the model you want to implement, allowing you to easily reason about things like how to efficiently calculate the next position the soldier is going to be based on the received input from the controller instead of preventing you to reason easily because you are too busy trying not to forget a 0. A crucial moment occurred with the jump from assembly language (a language very similar to machine code, it was the first programming language and it's CPU specific. Every assembly instruction directly translates into machine code) to C (which is portable among different CPUs and is at a higher level of abstraction than assembly: each line of C code represents many machine code instructions). This was a huge productivity increase for programmers, they no longer had to port programs between different CPUs, and they could think a lot more easily about the underlying models, leading to the continued complexity increase in software we've seen (and even demand) from the 1970s until today. The pending missing link is how to control what to do with that information and how to receive input from external sources, say displaying images in the screen or writing information to a hard drive, or printing an image on a printer, or receiving keypunches from a keyboard. This is all made possible by the rest of the hardware present in the computer which is controlled in a way similar to that of the CPU, you place data and instructions in certain transistors in the graphic card or the network card or the hard drive or the RAM. The CPU has instructions that will allow it to place some data or instruction into (or read information out of) the proper location of different pieces of hardware. Another relevant thing to the existence of what we have today is that all modern computers come with big programs called operating systems that manage all the basic stuff like talking to hardware and error handling, like what happens if a program crashes and so on. In addition, many modern programming environments come with a lot of already written code (standard libraries) to handle many basic tasks like drawing on a screen or read a file. This libraries will in turn will ask the operating system to talk to the hardware in its behalf. If these weren't available, programming would be a very very hard and tedious task as every program you write would have to create again code to draw a single letter on the screen or to read a single bit from each specific type of hard drive, for example. It seems I got carried away, I hope you understand something out of this :-) A: A computer programming language is actually a highly abstracted language that is converted down into a very very basic language that computers actually understand. Basically, computers really only understand machine language, which is a basic language implemented in binary (1's and 0's). One level above this is assembly language, which is a very primitive language that is at least human readable. In a high level language, we might have something like: Person.WalkForward(10 steps) In Machine code it would be: Lift Persons Left Foot Up Lean Forward Place Left Foot Down Lift Right Foot up Lean Forward Place Right Foot Down etc Now obviously, nobody wants to write programs that tell the computer every little repetitive thing to do so we have tools called compilers. A compiler takes a higher level language that is easier for a human to understand, and converts it down to machine code, so that the computer can run it. A: A good book that talks about computers for non-engineers is 'Code' by Charles Petzold. I don't recall exactly if it covers exactly your question, but I think so. If you are interested enough to go farther it's a good choice. Code http://ecx.images-amazon.com/images/I/11MYtZPhJEL._BO2,204,203,200_PIsitb-sticker-arrow-click,TopRight,35,-76_AA198_SH20_OU01_.jpg
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Champmol The Chartreuse de Champmol, formally the Chartreuse de la Sainte-Trinité de Champmol, was a Carthusian monastery on the outskirts of Dijon, which is now in France, but in the 15th century was the capital of the Duchy of Burgundy. The monastery was founded in 1383 by Duke Philip the Bold to provide a dynastic burial place for the Valois Dukes of Burgundy, and operated until it was dissolved in 1791, during the French Revolution. Called "the grandest project in a reign renowned for extravagance", it was lavishly enriched with works of art, and the dispersed remnants of its collection remain key to the understanding of the art of the period. Founding Purchase of the land and quarrying of materials began in 1377, but construction did not begin until 1383, under the architect Druet de Dammartin from Paris, who had previously designed the Duke's chateau at Sluis, and been an assistant in work at the Louvre. According to James Snyder his work at Champmol was "a somewhat conservative modification of the Late Gothic buildings of Paris". A committee of councillors from Dijon supervised the construction for the Duke, who was often elsewhere. By 1388 the church was consecrated, and most construction probably completed. The monastery was built for twenty-four choir monks, instead of the usual twelve in a Carthusian house, and two more were endowed to celebrate the birth in 1433 of Charles the Bold. These lived semi-hermitic lives in their individual small houses when not in the chapel. There would also have been non-ordained monks, servants, novices, and other workers. When founded, Champmol was "two arrow shots" outside the city gates, but is now inside the modern city boundaries. At this time the city had about 10,000 inhabitants and was the largest in Burgundy proper, though smaller than the cities of the territories in the Netherlands recently inherited by the Duke through his wife. But Burgundy was held more securely than the often turbulent cities in the north, and represented the senior title of the dynasty. Over sixty members of the Capetian House of Burgundy, whom the Valois had succeeded in 1361, only two decades earlier, had been buried at Cîteaux Abbey to the south of Dijon. Champmol was intended to rival Cîteaux, Saint-Denis, where the Kings of France were buried, and other dynastic burial places. Somewhat in contradiction to the Carthusian mission of tranquil contemplation, visitors and pilgrims were encouraged, the expenses of hospitality recompensed by the Dukes. In 1418 Papal indulgences were granted to those visiting the Well of Moses, further encouraging pilgrims. The ducal family had a private oratory overlooking the church (now destroyed), though their visits were in fact rare. The ducal accounts, which have fortunately survived, show major commissions for paintings and other works to complete the monastery continuing until about 1415, and further works were added after that at a slower rate by the Dukes and other donors. The accounts for Champmol have survived in sufficient detail that Martin Warnke synthesized from them a view of the emerging status of court artists, and "the autonomous consciousness of art and artists" that would distinguish the world of art in the Early modern period. Tombs of the Dukes The Valois dynasty of Burgundy had less than a century to run when the monastery was founded, and the number of tombs never approached that of their Capetian predecessors at Cîteaux – indeed there would hardly have been room in the choir of the church, where the monuments were. Only two monuments were ever erected, both in the same style with painted alabaster effigies with lions at their feet and angels with spread wings at their heads. Underneath the slab the effigies rested on, unpainted small (about 40 cm high) "pleurants" or mourners ("weepers" is the traditional English term) were set among Gothic tracery. These were described by Johan Huizinga in The Waning of the Middle Ages as "the most profound expression of mourning known in art, a funeral march in stone". Philip the Bold died in 1404, and his wife Margaret III, Countess of Flanders the following year. She had decided to rest her remains with those of her parents in Lille, and Philip had been planning a single monument for himself for over twenty years, having commissioned Jean de Marville in 1381. Work did not begin until 1384, and proceeded slowly, with Claus Sluter being put in charge in 1389. At the Duke's death in 1404, only two mourners and the framework were complete; John the Fearless gave Sluter four years to finish the job, but he died after two. His nephew and assistant, Claus de Werve took over and finished the sculptures in 1410. The effigies were painted by Malouel. John expressed a wish for his own tomb, this time a double one with his Duchess Margaret of Bavaria, to resemble that of his father, but nothing was done, even after his death in 1419, until 1435, and in 1439 de Werve died without having managed to find suitable alabaster. In 1443 a Spaniard, Jean de La Huerta, was contracted, and sent drawings for the effigies. He completed most elements, but not the effigies, before leaving Dijon in 1456. Yet another master was brought in, and the monument finally installed in 1470, by which time Philip the Good was himself dead. He seems to have made no provision for a monument for himself, and had initially been buried in Bruges, where he died. His son Charles the Bold had the remains brought back to Champmol after some years, but no monument was ever planned. Charles himself was relocated from Nancy to Bruges by his great-grandson Charles V in 1558. The second tomb repeats the design of the first, but with their execution spanning almost a century, stylistic differences can be seen, although some of the "pleurants" of the second tomb copy those of the first exactly. It is recorded that Philip the Good had a portrait of himself placed in the choir, where there were already those of the previous two Dukes. None of these are believed to have survived in the original, but surviving portraits may be copies of them. After the Revolution, and the sale of the monastery, the tombs were carefully moved to Dijon Cathedral in 1792, as their historic importance was recognised. But in the following year the cathedral was converted into a Temple of Reason and the effigies were vandalised, so that what are now seen are reconstructions. Many elements, including ten "pleurants", were removed by genteel looters. Gallery of the tombs Works of art from Champmol Champmol was designed as a showpiece, and the artistic contents, now dispersed, represent much of the finest monumental work, as opposed to illuminated manuscripts, of French and Burgundian art of the period. Without the works that remained at Champmol until the 18th century, Claus Sluter, Jacques de Baerze, Melchior Broederlam, Henri Bellechose, Jean Malouel, and Jean de Beaumetz would remain only names known from documentary records. Still at Champmol There are very important sculptures by Claus Sluter and his workshop on the church portal, including kneeling figures of Philip and his Duchess. The lower parts of the Well of Moses (Puits de Moise) survive, including six life-size figures of the Old Testament prophets who foretold the Messiah, most of the rest having been destroyed, apparently more by weathering than the Revolution. In Dijon museums Most items are in the Musée des Beaux-Arts, including its site in the former palace of the Dukes. The fragments from the Well of Moses and other similar pieces are in the Archaeological Museum. The following are only the main works in Dijon: Two painted and gilded carved wood retables, that are almost the only remaining works by the Flemish sculptor Jacques de Baerze, and also the only complete Netherlandish carved altarpieces before the late 15th century. The outer panels of the larger are the only surviving paintings by Melchior Broederlam, and highly important works for tracing the development of Early Netherlandish painting. Broederlam also painted and gilded the carvings by de Baerze. The tombs (in fact always cenotaphs) of the Dukes of Burgundy; the museum has the tombs of Philip the Bold and his son John the Fearless with his wife Margaret of Bavaria. The effigies are 19th-century reconstructions, from old drawings and prints, of the originals which were destroyed in the Revolution. About ten of the "pleurants" are also copies of originals liberated or lost. The funerary crown of Philip the Bold, in brass and glass. The head and torso of the crucified Christ from the Well of Moses. The Retable of Saint George, an early-15th-century painted altarpiece, probably donated by one of the monks, whose donor portrait appears at the foot of the crucified Christ. One of the crucifixions from the two hermitages added in 1433. Two altarpieces by Charles-André van Loo, which replaced older works (one the Retable of Saint George) in 1741. Elsewhere Louvre, the Martyrdom of Saint Denis by Henri Bellechose, the tondo of the Pietà by Jean Malouel, and one of 24 paintings of the crucifixion for the monks' hermitages by Jean de Beaumetz, all of which are the best known works of each artist. Washington, National Gallery of Art, the Annunciation by Jan van Eyck; the two other panels of the triptych recorded at Champmol in 1791 have been lost. Gemäldegalerie, Berlin, a large Madonna and Child, only rediscovered in 1960 and now on loan to the Gemäldegalerie, is attributed to Jean Malouel It is believed the Berlin picture was one wing of a diptych for Champmol, opposite a portrait of John the Fearless. Cleveland Museum of Art, the only other one of the 24 paintings by Jean de Beaumetz to survive, and four "pleurant" figures from Philip's tomb. Baltimore, Walters Art Museum, half of the "Antwerp-Baltimore Polyptych" c. 1400. Antwerp, the other three scenes of the "Antwerp-Baltimore Polyptych" Musée de Cluny, Paris, two bone and ivory relief triptychs by the leading Italian Embriachi workshop, donated by Duke Philip in 1393. Chicago (Art Institute of Chicago), the figure from a gilded and painted wood crucifix by de Baerze and Broederlam. Gallery Later history After the death in 1477 of Charles the Bold, Burgundy proper was recovered by force by France; the Kings, still descended from the Dukes via the Habsburgs and other routes, continued to support and occasionally visit the monastery. There was slight damage in the siege of Dijon in 1513 and in the French Wars of Religion, but essentially the monastery remained in its 15th-century state until it was decided to update it in the 1770s. The altarpieces of Saints Denis and George had been replaced by new paintings by Charles-André van Loo in 1741; both the new paintings are now in the Dijon museum. Remodelling in the 1770s involved the destruction of some medieval parts, but greater destruction followed the French Revolution. The monastery was suppressed in 1791, and on May 4, five days after the monks departed, the buildings and land were bought by Emmanuel Crétet (1747–1808), later to be Minister of the Interior under Napoleon with the title Comte de Champmol. He destroyed large parts of the buildings and the church. In 1833 the estate was bought by the local département as a mental asylum, and many new buildings erected. Today the buildings house a psychiatric hospital, and "aller à la chartreuse" is a local phrase for developing a mental disorder. The Sluter sculptures can be seen by visitors, and many of the contents are in the Dijon museum, with the tombs and carved retables housed in the former Palace of the Dukes. Notes References Dossier from the Dijon Museum (in French) Gelfand, Laura D. (2005), in Sarah Blick, Rita Tekippe, eds.: Y Me Tarde in Art and architecture of late medieval pilgrimage in Northern Europe and the British Isles, 2005, BRILL, Gelfand, Laura D.(1994); Fifteenth-century Netherlandish devotional diptychs; Origins and function, 1994, PhD dissertation, Case Western Reserve University. Lindquist, Sherry C.M.; "Women in the Charterhouse" in [https://books.google.com/books?id=jLmFbEdqBDUC&pg=RA1-PA177&dq=Champmol#PRA1-PA177,M1 Architecture and the Politics of Gender in Early Modern Europe], Ed. Helen Hills, Ashgate Publishing, Ltd., 2003, Snyder, James; Northern Renaissance Art, 1985, Harry N. Abrams, Vaughan, Richard; Philip the Bold, The Formation of the Burgundian State, Boydell Press, 2002, White, John. Art and Architecture in Italy, 1250 to 1400, London, Penguin Books, 1966, 2nd edn 1987 (now Yale History of Art series). Further reading Bibliography from the Cleveland exhibition Fliegel, Stephen N., et al. . Art from the Court of Burgundy: Patronage of Philip the Bold and John the Fearless, 1364–1419. Exhibition catalogue. Cleveland: Cleveland Museum of Art, 2004. Lindquist, Sherry C.M. Agency, Visuality and Society at the Chartreuse de Champmol, 2008, Ashgate, Monget, Cyprien. La chartreuse de Dijon, 3 vols, Montreuil-sur-Mer, Tournai, 1898–1905 Category:Carthusian monasteries in France Category:Arts in the court of Philip the Good Category:Buildings and structures in Dijon Category:History of Dijon Category:Gothic art Category:Burial sites of the House of Valois
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Fuel poverty in the United Kingdom In the United Kingdom fuel poverty is said to occur when, in order to heat its home to an adequate standard of warmth, a household needs to spend more than 10% of its income on total fuel use. Adequate warmth is generally defined to be in the main living room and in other occupied rooms during daytime hours, with lower temperatures at night, following the recommendations of the World Health Organization. Fuel poverty is not just about access to heating as the definition of fuel is taken to include all expenditure on domestic energy, including that used for hot water, cooling, lights and appliances. This definition is essentially that first established by Dr Brenda Boardman in her book entitled Fuel Poverty, first published in 1991, although fuel poverty has been the focus of political action since the early 1970s . Other definitions There are, however, a variety of different ways of considering household income when measuring fuel poverty. The UK definition does not, for example, take account of the amount that a household actually spends on fuel, nor the amount available for the household to spend on fuel after other costs have been met. The UK Government’s preferred definition of household income includes income from housing-related benefits in the calculation of household income. Other estimates of the extent of fuel poverty exclude benefits from household income. The charity National Energy Action (NEA) regards both these definitions as unacceptable and believes that disposable income (after the deduction of housing costs) should be used in the definition of fuel poverty. On 14 March 2011, the Secretary of State for Energy and Climate Change announced he had asked Professor John Hills of the London School of Economics to lead a review of the fuel poverty definition and target. The interim report of this independent review was published on 19 October 2011. On page 19 of the interim report, Hill suggests redefining a fuel poor household as one that has required fuel costs that are above the median level, and were they to spend that amount, would be left with a residual income below the official poverty line. No official action has yet been taken on this suggestion. Households in fuel poverty In early 2008 it was estimated by Energywatch that there were around 4.4 million households in fuel poverty in the UK, with just over 3 million in England alone. This was more than double the number in 2003. 2008 saw significant price increases of approximately 45% by energy companies on gas and electric. In early 2009 the companies declared they were to drop their prices, but only a 10% reduction was seen across the board and this did not happen, with the exception of British Gas, until March 31, once the worst of the winter was over. Research from NEA showed that as of March 2009 over 5 million households across the UK were living in fuel poverty. In April 2011 a YouGov survey indicated that the number of households in fuel poverty had risen to 6.3 million households, representing approximately 24% of all households in the UK. The UK Government's 2015 Fuel Poverty Report showed that 4.5 million households, or 17% of UK households, were in fuel poverty. Excess winter deaths Excess winter deaths are defined by the Office for National Statistics as the difference between the number of deaths during the four winter months (December to March) and the average number of deaths during the preceding autumn (August to November) and the following summer (April to July). Although the phenomenon of excess winter deaths is not unique to the United Kingdom, the incidence is markedly higher than for countries with similar climates and living standards. England has an 18% rise in deaths during the winter, on average, whereas Finland has a 10% increase, Germany and the Netherlands have 11%. Since 2000, excess winter deaths in England and Wales remained generally at around 25,000. For the period of 2007-2008 the number of excess winter deaths was 27,480 of which the Hill report estimated that around 10% were caused directly by fuel poverty. The winter of 2008-2009 was the coldest in 10 years, and the Office for National Statistics estimated there were a total of 36,700, an increase of 49% over the previous year, which represents a 23.8% rise in deaths during the winter. Lower totals in subsequent years were followed by a rise back to 31,100 excess deaths in the winter of 2012-2013, of whom 25,600 were aged 75 or older, resulting in the Conservative-Liberal Democrat coalition government being criticised for not exercising tighter control over UK energy companies. Deaths from hypothermia among UK pensioners almost doubled during the five years up to 2012, a time when several cold winters combined with large-scale increases in energy prices. The number of pensioners dying from hypothermia has nearly doubled in five years, a period when a succession of cold winters has been coupled with drastic rises in energy bills. Exposure to the cold does affect the number of winter deaths‚ but deaths from other cold related causes are very much more common than it is for the cold to kill people directly. In the main these deaths are from respiratory or cardio-vascular ailments. Overall deaths are from heart attacks‚ strokes‚ bronchial and other conditions‚ and may often occur several days after exposure to the cold. Spending too long in the cold will lower the body temperature which can often aggravate circulatory diseases‚ which can lead to strokes and heart attacks or respiratory illnesses such as bronchitis or pneumonia. Under the Climate Change and Sustainable Energy Act 2006 the Government is obliged to report annual progress in cutting the number of households in which one or more persons are living in fuel poverty. Action programmes The UK's main programme targeting fuel poverty is the Energy Company Obligation. The Home Heat Helpline - 0800 33 66 99 - can provide assistance to the following vulnerable groups: Advice on social tariffs – typically a 20% saving Access to the Priority Service Register, with free annual gas appliance safety checks, passwords for official gas and electricity-related callers. Third party, Braille, large print and talking billing Grants for free home insulation regardless of who owns the property and no means testing for the over 70s. Absolute right for them to receive free cavity wall and loft insulation or free top-ups to modern standards. Same help to all households in receipt of Attendance Allowance, Disability Living Allowance or Employment and Support Allowance (Incapacity Benefit) Single Parent Allowance or households with young children with an annual income of less than £14,600. Flexible payment options for customers in fuel debt A disconnection safety net, ensuring no vulnerable customer will be knowingly disconnected The Home Heat Helpline also recognises that those most in need of help are often those least able to access it so the helpline now accepts third party applications. Parliamentary Inquiry The UK Parliamentary Select Committee on Energy and Climate Change recently launched an inquiry on home energy efficiency in September 2015. See also Poverty Poverty in the United Kingdom Energy in the United Kingdom Energy efficiency in British housing Committee on Fuel Poverty References External links Chapter 1 the causes and effects of fuel poverty, The UK Fuel Poverty Strategy (2001), DTI National Energy Action: Fuel Poverty and Energy Efficiency Home Heat Helpline In the media Petrol Credits Category:Housing in the United Kingdom Category:Energy in the United Kingdom United Kingdom Category:Energy economics
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Q: Operator precedence in programming language In programming Language class, I learned operator precedence and associativity. The under is simple Context-Free-Grammar <expr> -> <expr> + <term> | <term> <term> -> <term> * <fact> | <fact> <fact> -> (<expr>) | a By using Context-Free-Grammar above, we can make the sentence a+a+(a+a) I think, the order of operation should be done as follow : (a+a) -> a+a then plus altogether. However, on lecture, the professor said both (a+a) -> a+a and a+a -> (a+a) order is right. Student's are in panic. Even in the sentence below, (a+a)+((a+a)) Both order ((a+a)) -> (a+a) then plus and (a+a) -> ((a+a)) is correct. He just said, after making parse tree, then converted to the assembly language so the order depends on Compiler. I don't understand his explanation. Is anybody can explain why there are two possible order?? A: Evaluation order is independent of grouping. If you need to calculate X + Y (where X and Y are sub expressions), it does not matter whether you first compute temp2 = Y and then temp1 = X or the other way around. At the end temp1 + temp2 has the same value. Sometimes it is more convenient to compute the right-hand argument first. (Maybe you already know it from a previous computation, for example.) If the computation of X or Y has a side effect, that might need to be taken into account. Some languages insist that side effects happen left to right; others allow any order. But in no case does parenthesis grouping affect the order of computation. It only determines what is computed.
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While you were out shopping Sunday for those last-minute holiday gifts, the Navy pushed ahead with its own vision of an underwater sugar plum: a fleet of “long endurance, transoceanic gliders harvesting all energy from the ocean thermocline.” And you thought Jules Verne died in 1905. Fact is, the Navy has been seeking—pretty much under the surface—a way to do underwater what the Air Force has been doing in the sky: prowl stealthily for long periods of time, and gather the kind of data that could turn the tide in war. The Navy’s goal is to send an underwater drone, which it calls a “glider,” on a roller-coaster-like path for up to five years. A fleet of them could swarm an enemy coastline, helping the Navy hunt down minefields and target enemy submarines. Unlike their airborne cousins, Navy gliders are not powered by aviation fuel. Instead, they draw energy from the ocean’s thermocline, a pair of layers of warm water near the surface and chillier water below. The glider changes its density, relative to the outside water, causing the 5-foot (1.5m)-long torpedo-like vehicle to either rise or sink—a process called hydraulic buoyancy. Its stubby wings translate some of that up-and-down motion into a forward speed of about a mile (1.6 km) an hour in a sawtooth pattern. As it regularly approaches the surface, an air bladder in the tail inflates to stick an antenna out of the water so it can transmit what it has learned to whatever Captain Nemo dispatched it to the depths. Much of the work such gliders do is oceanographic in nature, collecting data about the water’s temperature, salinity, clarity, currents and eddies. Such information is critical for calibrating sonar to ensure it provides the most accurate underwater picture possible. But there are additional efforts underway to convert such data into militarily-handy information. Webb Research Slocum Gliders rise and fall as they traverse the ocean’s depths, transmitting what they learn via tail-mounted antennas that periodically break through the water’s surface. The Navy’s Sunday contract announcement added a scant $203,731 to a contract it has with Teledyne Benthos, Inc., for continued “research efforts” into its Slocum Gliders (named for Captain Joshua Slocum, who sailed alone around the world in a 37-foot sloop between 1895 and 1898). “Carrying a wide variety of sensors, they can be programmed to patrol for weeks at a time, surfacing to transmit their data to shore while downloading new instructions at regular intervals, realizing a substantial cost savings compared to traditional surface ships,” the company’s Webb Research division says. The Webb unit is located in East Falmouth, Mass., and its Slocum Glider is the brainchild of Douglas Webb, a former researcher at the nearby Woods Hole Oceanographic Institution. In 2009, the Navy issued a $56.2 million contract for up to 150 of the “Littoral Battlespace-Sensing” gliders to be delivered by 2014. The Navy has said it is investing in the field because such information could prove vital “for mine countermeasures and other tasks important to expeditionary warfare. . .ultimately reducing or eliminating the need for sailors and Marines to enter the dangerous shallow waters just off shore in order to clear mines in preparation for expeditionary operations.” A NATO report last year examined the feasibility of launching Slocum Gliders from torpedo tubes instead of T-AGS oceanographic surveillance ships. “Operating gliders from submarines represents a step forward to embedding this technology into naval operations,” it said. “Unlike surface ships, submarines are stealth platforms that could transit denied areas while releasing a glider fleet.” Navy Captain Walt Luthiger, a submariner, said an exercise using such gliders proved their mettle in yet another arena. “The environmental information provided by the gliders has proved valuable,” he told NATO public affairs in 2011, “and helped everyone in that very difficult job of finding submarines that don’t want to be found.” Astronaut Scott Carpenter wrote a book a long time ago called, "The Steel Albatross" that featured a military stealth submarine that was propelled by gliding. They would alternately fill and blow the ballast tank and use the wings to fly the sub. With minimal thrusters there were no prop noises. and have you heard of the new "God particle" weapon ???!!!!! i know its revolutionary but when you shoot it at another person it does not kill him but actually shows him your love and forgiveness!!!!!! wtf? http://hereitis.ws/JesusChristAdvertisement.htm !!!!!!! When wars begin they are usually a surprise and then are conducted with the latest in obsolete technology and tactics. Right now there are researchers looking for vulnerabilities in our carriers, submarines and stealth aircraft, some of it by allies. Part of the dream of Socialism was that the solidarity of workers would end war, the World Court would arbitrate conflicts away and for a while the interlocking dynasties of Victoria's children supposedly secured peace. After WW1 we tried The League of Nations, men of good faith negotiated with Hitler for peace in our time, while men of ill will negotiated the Treaty of Non-aggression between Germany and the Union of Soviet Socialist Republics,and after WW2 we tried the UN. War will always be with us, better minds than ours have struggled to end it, limit it and civilize it, yet war remains Hell. No one ever wins a war, but there are losers, it is better to do everything in your power not to be a loser. Why is it we feel the need to let everyone on the planet know what we are doing militarily? It just doesn't make sense to let our enemies know what we have, and what we are working on to defend ourselves. As an American citizen, would I like to know? Sure I would, but it is not necessary to know every little advancement we come up with, some things are just better left alone, and not publicized for the good of all of us. The statement "they draw energy from the ocean’s thermocline, a pair of layers of warm water near the surface and chillier water below" is incorrect. There is no energy thermodynamically available at the thermocline, which is in thermodynamic equilibrium. The energy that 'propels' the device is the energy which changes its density, which must compress a gas-filled chamber on board the glider. The energy running the compressor must be carried on the device. Gravity does the rest through Archimedes' Principle. Smart, real smart. First they come to the surface to transmit which makes them a navigation hazard and having been on a boat that came to periscope depth only to crash dive because there was a yacht with wide eyed people dead ahead, it could be a real problem and then secondly, the big one, the current speeds along most coast line is far in excess of the one mile per hour speed. Guess they are only a one way ticket. I can see it now a huge recovery program in the arctic or antarctic. Maybe we could train penguins to recover them. ';-) This is old news. Read about it in magazines years ago. Saw it on the History Channel in the last year too...it is interesting though...no telling what they are really doing now. Skunk works for the oceans? 14And the heaven departed as a scroll when it is rolled together; and every mountain and island were moved out of their places. 15And the kings of the earth, and the great men, and the rich men, and the chief captains, and the mighty men, and every slave, and every free man, hid themselves in the dens and in the rocks of the mountains; 16And said to the mountains and rocks, Fall on us, and hide us from the face of him that sits on the throne, and from the wrath of the Lamb: I remember when I was little, every now and then, while watching the news my 80+ grandmother used to say "I'm glad I'm going to die soon.". I used to scold her for wishing to leave me. Well now, many years later. Hmmmphhh. Add a muffler, Hellfire misslies, and 4(pi) steradian retina-melting Nd:glass or Nd:YAG lasers. Teach them how to parachute from a Lockheed C-5M Super Galaxy. Navy? Less than one knot net on a good day? "ACK! THBBFT!" Where is the paint locker? @RicBov Oh yeah , the now more than half a trillion of dollars wasted every year on the most dangerously bloated and over-sized military in the world is a "brilliant use of taxpayer money" according to some. Ah delusion. Meanwhile the US is the most unequal country among all developed nations and have the most costly while poorly ranked healthcare system. But hey life is question of priorities. If they are actively patrolling our shores, then they are actively wasting their money. You know, the Soviets used to bring factory fishing vessels within a few miles from US shores, draining our fish stocks. THAT was a problem, and resulted in the Magnusson-Stevens Act, which extended our sovereign waters from just a couple miles to like 30 miles out from US shores, I believe. That was a good solution to a material problem. Anyway, you're beating the war drums about China spying on us. Perhaps I'm being naive here, but suppose China were patrolling US waters, like 29 miles out - so freaking what? As long as our Coast Guard and our military is doing its job, and so long as China isn't attacking us or depleting our resources, and so long as it can't gather valuable intel on us dozens of miles out as see, then what exactly is the problem? I suppose if China were a material threat, these drones would be useful, but really the drones seem better for fisheries monitoring, for oceanographic study, or even for LNG or hydrocarbon prospecting. It seems like their immediate uses would be mostly nonmilitary. @Freedom12You sure would like to think so, but I have my reservations that they are smart enough to be that cunning. Remember that the Navy is still part of the Government, and they do almost nothing right. There is no need for anyone outside the U.S. Navy to know anything about a program like this, it just boggles the mind to know they use our taxpayers dollars to come up with weapons of war like this, and then turn around and give all their secrets away. I for one do not like my tax dollars spent this way. have they ever heard of that old saying "Only on a need to know basis"
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High Dilution Principle In organic chemistry, the High Dilution Principle is a strategy for some macrocyclization reactions, i.e. the synthesis of macrocycles. Unlike the synthesis of 5- and 6-membered rings, the preparation of larger rings competes unfavorably with polymerization reactions. Polymers arise from coupling of long chain precursors. Such reactions are disfavored when the acyclic compounds are dilute. Although high dilution reactions can be conducted in a batch reactor with large volumes of solvent, a more practical implementation entails slow addition of reactants, under conditions that the reactants are more rapidly consumed than the rate of addition. Typically, additions use one or more syringe pumps. Illustrative is the synthesis of thiacyclopentadecane from 1,14-dibromotetradecane and sodium sulfide in 45% yield: BrCH2(CH2)12CH2Br + Na2S → (CH2)14S + 2 NaBr References Category:Carbon-carbon bond forming reactions
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Flag of the Second Spanish Republic The flag of the Second Spanish Republic, known in Spanish as , was the official flag of Spain between 1931 and 1939 and the flag of the Spanish Republican government in exile until 1977. History The Spanish republican flag began to be used on April 27, 1931, thirteen days after municipal elections results led to the abolition of the monarchy and the proclamation of the Second Spanish Republic. This same flag had been previously displayed by certain Republican groups as an alternative to the red-and-yellow flag that was identified with the Bourbon monarchy in Spain. As a result of this previous use, the young republic proclaimed in 1931 eagerly adopted this symbol. The Republican flag was adopted on April 27 and presented to the army of the nation on May 6 with the following words: "The national uprising against tyranny, victorious since April 14, has hoisted a flag that is invested by means of the feelings of the people with the double representation of the hope of freedom and of its irreversible triumph." The Republican flag was formed by three horizontal bands of the same width, red, yellow, and murrey (mulberry-coloured). The National Flag would have the Spanish Republican coat of arms at the centre (quarterly of Castile, Leon, Aragon and Navarre, enté en point for Granada, ensigned by a mural crown, between the two Pillars of Hercules). This coat of arms originated in 1868 and had been used then by the Provisional Government and later by the First Spanish Republic. The civil ensign or merchant flag would be a simple tricolour without the coat of arms. The term "la tricolor" to refer to the flag is reminiscent of the French tricolor which, since the French Revolution of the late 18th Century, has made a flag composed of three equal strips into the symbol of a Republic. However, having horizontal strips rather than vertical ones, as in the French flag, made it possible to preserve many elements of the previous Spanish flag, used during centuries of Monarchial rule. During the Civil War there was also a military version of the flag with proportion 2:3 and without the coat of arms used by Republican Army units in different locations. Despite not displaying the arms, this plain flag did not correspond to the civil ensign approved in 1931 for the use of merchant ships. The International Brigades added a three-pointed red star to the yellow band of the military Republican flag. The simplified military flag of the Second Spanish Republic was also used by the Spanish Maquis between the end of the Spanish Civil War and the early 1960s, and later by the Spanish National Liberation Front (FELN). Versions of this flag were used in the 1970s by the radical anti-Francoist groups Revolutionary Antifascist Patriotic Front (FRAP) and First of October Anti-Fascist Resistance Groups (GRAPO). The Republican flag is now widely used by trade unions and left-wing political organizations, such as United Left, the Marxist-Leninist Party (RC) and some factions of the Spanish Socialist Workers' Party. It is also used by republican platforms. Colours The Spanish Republican Flag has three colours: red, yellow, and dark purple. The third colour, dark purple (), represents Castile and León by recalling the Pendón Morado, the ancient armorial banner of Castile. The colours of red and yellow symbolise the territories of the former Crown of Aragon. These three colours symbolised a new era for Spain in which no part thereof was excluded and all Spaniards were represented. Morado Morado, which is a generic word denoting the colour purple or violet, was previously a familiar colour in Spain because it is one of the Catholic liturgical colours that is displayed on vestments, altar cloths, and other ecclesiastical textile furnishings to signify certain seasons of the Catholic liturgical year, and, being a historically Catholic nation, this colour had annual and public use throughout Spain. Also, it was used in antiquity as the heraldic colour of the Kingdom of Castile. The coat of arms of the Kingdom of León bore a purple lion rampant and the flag reputed to have been used in the Revolt of the Comuneros displayed a yellow castle on a purple background. Morado, however, was and is prone to variations in hue and fading from time and use, which often resulted in "morado" denoting a range of hues of purple, which presently are considered distinct colours/hues, e. g. crimson or maroon. Because it is rarely present on flags, in practice the morado of the lowest band of the Flag was coloured violet, purple (purpure), or even lilac, contingent on available materials and dyes. Controversies Spanish monarchists resented the morado of the new tricolored flag and a famous soleá was composed when the Flag began to be used. These verses also indirectly expressed dissatisfaction for the reforms of the new republican government: Since the restoration of the monarchy in the last quarter of the 20th century, some authors contradict previous Spanish historians by arguing that the Castilian Pendón Morado never existed or that it was actually coloured red. Until recently the official badge of the Real Madrid C.F. had a purple band based either on the Castilian or Spanish republican colours which was added after the proclamation of the Second Spanish Republic in 1931. The colour of the band was changed from morado to navy blue in 2001. Depictions, derivatives and variants Civil use Military use Present-day use See also Flag of Spain Coat of arms of the Second Spanish Republic Second Spanish Republic Himno de Riego Madrid Distinction References External links Armada Española - Segunda República (1931 - 1939) The Flags of Spain. Flags of the World Asturias Republicana Ministerio de Defensa - Insignias Jefes de Estado; Presidente de la II República Second Spanish Republic National Anthem Images La bandera de la República Española ondea por primera vez en París La Bandera Republicana ondea en París Category:National symbols of Spain Second Spanish Republic Category:Second Spanish Republic Category:Republicanism in Spain Second Spanish Republic
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Can warmwater streams be rehabilitated using watershed-scale standard erosion control measures alone? Degradation of warmwater streams in agricultural landscapes is a pervasive problem, and reports of restoration effectiveness based on monitoring data are rare. Described is the outcome of rehabilitation of two deeply incised, unstable sand-and-gravel-bed streams. Channel networks of both watersheds were treated using standard erosion control measures, and aquatic habitats within 1-km-long reaches of each stream were further treated by addition of instream structures and planting woody vegetation on banks ("habitat rehabilitation"). Fish and their habitats were sampled semiannually during 1-2 years before rehabilitation, 3-4 years after rehabilitation, and 10-11 years after rehabilitation. Reaches with only erosion control measures located upstream from the habitat measure reaches and in similar streams in adjacent watersheds were sampled concurrently. Sediment concentrations declined steeply throughout both watersheds, with means > or = 40% lower during the post-rehabilitation period than before. Physical effects of habitat rehabilitation were persistent through time, with pool habitat availability much higher in rehabilitated reaches than elsewhere. Fish community structure responded with major shifts in relative species abundance: as pool habitats increased after rehabilitation, small-bodied generalists and opportunists declined as certain piscivores and larger-bodied species such as centrarchids and catostomids increased. Reaches without habitat rehabilitation were significantly shallower, and fish populations there were similar to the rehabilitated reaches prior to treatment. These findings are applicable to incised, warmwater streams draining agricultural watersheds similar to those we studied. Rehabilitation of warmwater stream ecosystems is possible with current knowledge, but a major shift in stream corridor management strategies will be needed to reverse ongoing degradation trends. Apparently, conventional channel erosion controls without instream habitat measures are ineffective tools for ecosystem restoration in incised, warmwater streams of the Southeastern U.S., even if applied at the watershed scale and accompanied by significant reductions in suspended sediment concentration.
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When we hear the words, semiconductor device, we may think first of the transistors in PCs or video game consoles, but transistors are the basic component in all of the electronic devices we use in our daily lives. Electronic systems are built from components such as transistors, capacitors, wires and other electronic devices such as light emitting diodes and semiconductor lasers. These components are typically integrated into a single chip made of a semiconductor material. Advanced courses go more deeply into semiconductor theory, device physics, fabrication processes, and advanced and special purpose devices, such as heterostructure devices, power devices, and optoelectronic devices. 10 11 This nanoHUB "topic page" provides an easy access to selected nanoHUB Semiconductor Device Education Material that is openly accessible and usable by everyone around the world. 12 13 We invite you to participate in this open source, interactive educational initiative: 14 15 * [http://www.nanohub.org/contribute/ Contribute your content] by uploading it to the nanoHUB. (See "Contribute Content") on the nanoHUB mainpage. 16 * Provide feedback for the items you use on the nanoHUB through the review system. (Please be explicit and provide constructive feedback.) 17 * Let us know when things do not work for you - file a ticket through the nanoHUB "Help" feature on every page 18 * Finally, let us know what you are doing and [http://www.nanohub.org/feedback/suggestions/ your suggestions] improving the nanoHUB by using the "Feedback" section, which you can find under "[http://www.nanohub.org/support/ Support]" 19 20 Thank you for using the nanoHUB, and be sure to [http://www.nanohub.org/feedback/success_story/ share your nanoHUB success stories] with us. We like to hear from you, and our sponsors need to know that the nanoHUB is having impact. [[Image(/site/resources/tools/kronig_penney/allowed_bands_step_well.png, 120 class=align-right)]] The [/resources/5065 Periodic Potential Lab in ABACUS] solves the time independent Schroedinger Equation in a 1-D spatial potential variation. Rectangular, triangular, parabolic (harmonic), and Coulomb potential confinements can be considered. The user can determine energetic and spatial details of the potential profiles, compute the allowed and forbidden bands, plot the bands in a compact and an expanded zone, and compare the results against a simple effective mass parabolic band. Transmission is also calculated through the well for the given energy range. [[Image(/site/resources/tools/strainbands/strainbands2.png, 120 class=align-right)]] [/resources/5065 StrainBands in ABACUS] uses first-principles density functional theory within the local density approximation and ultrasoft pseudopotentals to compute and visualize density of states, E(k), charge densities, and Wannier functions for bulk semiconductors. Using this tool, you can study and learn about the bandstructures of bulk semiconductors for various materials under hydrostatic pressure and under strain conditions. Physical parameters such as the bandgap and effective mass can also be obtained from the computed E(k). We note here that the bandgaps obtained with DFT-LDA are underestimated, by about a factor of two for some semiconductors (including Si and GaAs), as is well known. + 67 - + 68 - Exercises: + 69 - + 70 - * [[Resource(4880)]] + 71 72 [[Div(start, class=clear)]][[Div(end)]] 73 74 75 == Bulk Semiconductors == 76 === [/tools/abacus Carrier Statistics Lab] === 77 78 [[Image(/site/resources/2008/01/03885/cd_pg1.jpg, 120 class=align-right)]] The [/resources/5065 Carrier Statistics Lab in ABACUS] demonstrates electron and hole density distributions based on the Fermi-Dirac and Maxwell Boltzmann equations. This tool shows the dependence of carrier density, density of states and occupation factor on temperature and fermi level. User can choose between doped and undoped semi-conductors. Silicon, Germanium, and GaAs can be studied as a function of doping or Fermi level, and temperature. It is supported by a [/resources/3878/ homework assignment] in which Students are asked to explore the differences between Fermi-Dirac and Maxwell-Boltzmann distributions, compute electron and hole concentrations, study temperature dependences, and study freeze-out. 79 80 Exercises: 81 - + * [[Resource(5146)]] 82 - * [[Resource(5146)]] + * [[Resource(4892)]] 83 - + * [[Resource(5197)]] 84 - * [[Resource(4892)]] + 85 - + 86 - * [[Resource(5197)]] + 87 88 89 === [/tools/abacus Drift Diffusion Lab] === 90 91 [[Image(/site/resources/tools/semi/excess_carrier_profile_light_top.png, 120 class=align-right)]] The [/resources/5065 Drift Diffusion Lab in ABACUS] enables a user to understand the basic concepts of DRIFT and DIFFUSION of carriers inside a semiconductor slab using different kinds of experiments. Experiments like shining light on the semiconductor, applying bias and both can be performed. This tool provides important information about carrier densities, transient and steady state currents, fermi-levels and electrostatic potentials. It is supported by two related homework assignments [/resources/4191/ #1] and [/resources/4188/ #2] in which Students are asked to explore the concepts of drift, diffusion, quasi Fermi levels, and the response to light. [[Image(/site/resources/tools/adept/adept2.png, 120 class=align-right)]] [/tools/adept/ ADEPT] is not supported within ABACUS, since it is a research-oriented tool that enables the study of solar cells for various material systems. A [/site/resources/2007/05/02659/adoc.pdf Reference Manual] and a [/site/resources/2007/05/02660/adept_heterostruct_tutorial.pdf ADEPT Heterostructure Tutorial] are available. The interface is not a simple point-and-click interface as for example the PN junction lab, but simulation commands are entered in a command-like fashion. 126 127 [[Div(start, class=clear)]][[Div(end)]] 128 129 == Bipolar Junction Transistors (BJT) == 130 131 === [/tools/abacus/ Bipolar Junction Lab] === 132 133 [[Image(/site/resources/tools/bjt/5_BJTenergy_nonequil.gif, 120 class=align-right)]] The [/tools/abacus/ Bipolar Junction Lab in ABACUS] allows Bipolar Junction Transistor (BJT) simulation using a 2D mesh. It allows user to simulate npn or pnp type of device. Users can specify the Emitter, Base and Collector region depths and doping densities. Also the material and minority carrier lifetimes can be specified by the user. It is supported by a [/resources/4185/ homework assignment] in which Students are asked to find the emitter efficiency, the base transport factor, current gains, and the Early voltage. Also a qualitative discussion is requested. 134 135 [[Div(start, class=clear)]][[Div(end)]] 136 137 Exercises: 138 * [[Resource(5199)]] 139 * [[Resource(5193)]] 140 * [[Resource(5083)]] 141 142 143 == MOS Capacitors == 144 145 === [/tools/abacus/ MOScap] === 146 147 [[Image(/site/resources/tools/moscap/moscap.jpg, 120 class=align-right)]] The [/tools/abacus/ MOScap Tool in ABACUS] tool enables a semi-classical analysis of MOS Capacitors. Simulates the capacitance of bulk and dual gate capacitors for a variety of different device sizes, geometries, temperature and doping profiles. 148 149 [[Div(start, class=clear)]][[Div(end)]] 150 151 Exercises: 152 * [[Resource(4855)]] 153 * [[Resource(5185)]] 154 * [[Resource(5187)]] 155 * [[Resource(5189)]] 156 * [[Resource(5087)]] 157 158 159 === [/tools/schred/ Schred] === 160 161 [[Image(/images/tool/schred/schred.jpg, 120 class=align-right)]] [/tools/schred/ Schred] is not formally supported in ABACUS. It contains more advanced quantum mechanical concepts and is a nanoHUB contributed tool. It calculates the envelope wavefunctions and the corresponding bound-state energies in a typical MOS (Metal-Oxide-Semiconductor) or SOS (Semiconductor-Oxide-Semiconductor) structure and a typical SOI structure by solving self-consistently the one-dimensional (1D) Poisson equation and the 1D Schrodinger equation. 162 163 [[Div(start, class=clear)]][[Div(end)]] 164 165 Exercises: 166 * [[Resource(4900)]] 167 * [[Resource(4902)]] 168 * [[Resource(4904)]] 169 * [[Resource(4794)]] 170 * [[Resource(4796)]] 171 172 173 == MOSFETs == 174 175 === [/tools/abacus/ MOSfet Lab] === 176 177 [[Image(/site/resources/tools/mosfet/mosfet.jpg, 120 class=align-right)]] The [/tools/abacus/ MOSfet Lab in ABACUS] tool enables a semi-classical analysis of current-voltage characteristics for bulk and SOI Field Effect Transistors (FETs) for a variety of different device sizes, geometries, temperature and doping profiles. 178 179 Exercises: 180 * [[Resource(4906)]] 181 * [[Resource(5104)]] 182 * [[Resource(5191)]] 183 * [[Resource(5085)]] 184 185 186 187 == About ABACUS Constituent Tools == 188 The Assembly of Basic Applications for Coordinated Understanding of Semiconductors (ABACUS) has been put together from individual disjoint tools to enable educators and students to have a one-stop-shop in semiconductor education. It therefore benefits tremendously from the hard work that the contributors of the individual tool builders have put into their tools. 189 190 As a matter of credit, simulation runs that are performed in the ABACUS tool are also credited to the individual tools, which help the ranking of the individual tools. We do also count the number of usages of the individual tools in the ABACUS tool set, to measure the ABACUS impact and possibly also improve the tool. 191 192 In the description above we do not refer to the individual tools since we want to guide the users to the composite ABACUS tool. We cite the individual tools here explicitly so they are being given the appropriate credit and on their rspective tool pages are being linked to this ABACUS topic page.
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A device can typically include one or more central processing units (CPU) that are used to process a wide variety of instructions for the device. Each of the CPUs is hardware that carries out the instructions of a program by performing the basic arithmetical, logical, and input/output operations of the device. For example, the CPU can be used to process different tasks that are running on the device. Each of these CPU operations will cause the device to consume power that leads to heat being generated by the device. This generated heat can add to a thermal load being applied to the device. An excessive thermal load can affect the device performance and, in extreme cases, can lead to a device shutdown. Existing devices can mitigate the thermal load by reducing the CPU operations globally for all processes, regardless of whether the CPU operations are for a batch process or a process supporting a user interface operation.
3.296875
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Industrial and commercial storage tanks facilitate trade and are an integral part of modern commerce. From water processing and dry commodities to oil and frac sand, storage tanks are an essential component of a variety of industries. Yet despite the widespread use and impact of storage tanks, tank production remains much the same as it was 100 years ago. Sheets are cut from steel plates of varying thickness and manipulated to match the desired tank dimensions. One of the first steps in building a storage tank is to properly position the metal panels that will be welded together to form the tank itself. The metal panels are often large, heavy steel sheets that are moved into place by a crane. While the metal sheet is still attached to the crane, workers help guide the sheet into the proper location so that the metal sheets may be welded together. To stay on schedule, workers must position the metal sheets quickly so that the crane can lift more metal sheets to be laid in position. Because most tank building takes place outdoors, workers are subjected to nature's elements. Wind, rain, and other weather conditions make the positioning of metal sheets difficult and unsafe. For example, high winds often cause metal sheets suspended from a crane to sway. Additionally, heavy rain can cause the workers' tools to slip. Even in good weather, the metal panel will rarely be correctly positioned after it is released from the crane. Workers must therefore exert great force and strength to move the panels into place. Workers currently use various types of crowbars to align the large steel panels. This process is extremely labor intensive and time consuming. It requires workers to bend down and exert great amounts of pressure on their backs, legs, and arms as they push and pry the metal sheets. In inclement weather, the task of moving the large metal sheets becomes even more difficult because the crowbars are slippery. Crowbars are the most common method of metal plate alignment in the storage tank industry. Dowel pins, or locating pins, provide another method of plate alignment. The pins are strategically placed so two pieces of sheet metal are aligned properly until they are welded or bolted together. After the tank is assembled, the dowel pins are removed and the holes are sealed with a weld. Although dowel pins are useful for more exact metal sheet positioning, workers still must use crowbars or similar methods to position the metal in place before inserting the dowel pins. Furthermore, the dowel pins must be removed and the holes welded over before the tank is finished. Additionally, the weight of the large metal sheets may bend or break the dowel pins. Dowel rods thus slow the process of tank building, and the dowel rods themselves are useful only for holding the sheets together, not for positioning the sheets in place. Embodiments of the invention will not be limited to storage tank production. A version of the invention will generally find utility in any application that requires incremental positioning. One embodiment of the invention is aimed at incrementally moving large and heavy pieces of metal, and a version of the invention may be utilized in many applications in which the incremental positioning of metal is desired. Such applications include, but are not limited to, ship and vessel building, defense building applications, aerospace and airplane construction, and the like. In all industries, the current method of metal positioning is based on the highly labor intensive use of crow and pry bars. Thus, a need exists in the art for a device that eases the process of positioning large metal sheets. Furthermore, a device that utilizes tools already in use is preferred, and, as in all fields, advancements in the art are desired.
3.765625
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Bread-making is a very old art. Over the centuries, a great number of techniques has been developed to impart a specific flavor and taste to the typical product of fermentation of flour mixed with water and certain yeast and bacteria. It has long been known, for example, to utilize the nutritional value and flavor qualities of milk in bread making processes. Improving and enhancing the flavor of bakery products is still a great concern for cereal scientists. Bread processes have significantly shortened and fermentation times as well as mixing times are kept at minimum. Therefore, microorganisms involved in panary fermentation do not have time to produce much flavoring materials in dough. In recent years, some bread-making processes have undergone numerous changes to satisfy the consumer who is now more open to diversified products such as bagels, muffins and sourdough bread. The latter is a bakery product with a very unique flavor. The product is particularly popular in the San Francisco area. A traditional process of making sourdough bread consists of providing wheat flour (rye may be used) and varying proportions of water, and allowing the mixture to ferment at room temperature until optimum flavor and acidity develops. The "starter" mixture is reworked regularly by adding flour and water to ensure that it contains sufficient amounts of fermentable compounds. Fermentation can therefore take several days and the resulting leavening agent is incorporated into the dough in quantities varying from 15 to 80% on the basis of flour. This multistage process is still widely used today despite its deficiencies, i.e., duration, inconsistency of product quality and difficult process control. A number of approaches have been proposed to modify the sourdough process, or, in general, to develop bakery products with different taste, or flavorants for the bread making process. Adding flavoring compounds (commercial bases) to the dough is one strategy employed to reduce fermentation time (Ziemke and Glabe, U.S. Pat. No. 4,034,125). The latter proposal serves to reduce the production time and assure better control over the finished product, the trade-off being the taste of bread produced in this fashion. Kline (U.S. Pat. No. 4,140,800) proposes to use a freeze-dried culture of lactobacilli (L. sanfrancisco) to better control sourdough production and to reduce sourdough preparation time to approximately 18 to 10 hours. Others have tried to imitate the sourdough process by adding acid whey power and vinegar to the dough (Shenkenberg, et al., 1972, Food Prod. Dev. 6(1), 29-30, 32). Another means of enhancing the flavor of bread is to use 4-6% (flour basis) non-fat milk solids (NFMS) during bread-making. To cut costs, NFMS may be replaced, at least in part, with whey powder which is less expensive and also improves to some extent the color, aroma and taste of the finished product. Jaeggi, et al., U.S. Pat. No. 4,001,437, propose to manufacture aroma substances, or flavorants, by heating a liquid product, obtained from carbohydrate-containing milk products by enzymatic proteolysis and/or by lactic acid fermentation. The final product has a bread-crust flavor reminiscent of roasted cheese. Hill, U.S. Pat. No. 3,846,561, incorporates yogurt in the dough from which baked products are prepared. Jaeggi and Hill processes involve bacteria of the genera Lactobacillus or Streptococcus. For yoghurt (Hill process), Lactobacillus delbrueckii subsp. bulgaricus and Streptococcus thermophilus are the specific bacteria to be used.
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Suicide in Ireland Suicide in Ireland has the 17th highest rate in Europe and the 4th highest for the males aged 15–24 years old which was a main contributing factor to the improvement of suicides in Ireland (World Health Organisation, 2012). On average, adjusted for age, The Central Statistics Office provided the overall suicide rate has a decreasing trend, which is from 13.5 per 100,000 population in 2001 to 8.5 in 2016 (The National Suicide Research Foundation, 2016). The suicide rate was significantly higher in males than females (OECD, 2018). Also, Irish young men and women suicide rate also had recorded the highest rate in Europe (Richardson et al., 2013; European Child Safety Alliance, 2014). Hanging is the most common suicide method that people in Ireland used (Departments of Public Health, 2001). The second common method is drowning (Departments of Public Health, 2001). Then, shooting, and overdose respectively (Departments of Public Health, 2001). WHO stated that strong partnership such as media, school, and the government should be working together and giving support to prevent suicide (WHO, 2014). __TOC__ Statistics The National Suicide Research Foundation (NSRF) has kept a record on the Irish suicide rate. Overall, Ireland has the trend of decreasing suicide rate in recent years. From 2011, the population has decreased from 12.1 per 100,000 population to 8.5 per 100,000 population in 2016 (NSRF, 2016). Youth suicide as a main contributing factor to the Irish suicide rate increased. A report (Richardson et al., 2013) stated that Irish young males had the highest number of suicides in Europe from the EU context, while another report showed Irish young females also experienced the highest suicide rate in Europe in 2018 (European Child Safety Alliance, 2014). The National Suicide Research Foundation (2016) indicated the highest rate of suicide in Ireland for male was 30 per 100,000 population, aged 20–24, while that of female was approximately 7 per 100,000 population aged 50–54 between 2007 and 2015. Male suicide rate was significantly higher than female, especially in 2011, where it was around 5 times higher in male than female (NSRF, 2016). A report in 2018 indicated that in 400 suicides, 8 of 10 are men (Orla, 2018). Common Methods A national study in Ireland in 2001, showed the most common method that people used to suicide in Ireland is hanging (Departments of Public Health, 2001; Biddle et al., 2010). Other suicide methods commonly used in Ireland included drowning, shooting, and overdose respectively (Departments of Public Health, 2001). Gender For gender, males were more likely to kill themselves in a more violent way such as hanging or shooting, while females were more apparent to drown, overdose or poison themselves in order to suicide (Departments of Public Health, 2001). Age For ages, younger people aged 15–24 were more likely to use hanging to suicide, while adults aged 25–34 years old were found more common in drug overdose and self-poisoning (Arensman et al., 2016). Therefore, the population of suiciding by hanging would reduce when people got older, and yet increased in firearms suicide (Arensman et al., 2016). Risk Factors Unemployment Unemployment was strongly associated with Ireland suicide rate. According to the studies, the unemployment rate in Ireland had a decreasing trend from January 2012 of 16% to January 2016 which is 9% (Eurostat, 2019). At this period, the Ireland suicide rate was also decreasing from 2012 (11.8 per 100,000 population) to 2016 (8.5 per 100,000 population) (NSRF, 2016). The result showed a higher unemployment rate contributed to a higher suicide rate in Ireland. People who were unemployed usually experienced health problems that made them unable to work, thereby increased their stress of life and financial difficulties, leading to deceleration of self-esteem (Preti & Miotto, 1999). Moreover, high levels of stress and financial difficulties might pose negative impacts on their mental health, which caused attempt to commit suicide and self-harm (MFHA, 2016). However, limitations do exist. It was difficult to understand whether unemployment contributed to the promotion of committing suicide (Departments of Public Health, 2001). Between 2002-2008, the unemployment rate is significantly lower than in other years, but the suicide rate was not influenced by the unemployment rate (Eurostat, 2019; NSRF, 2016). Therefore, other risk factors should also be considered in promoting suicide intentions in Ireland. Mental illness Mental illness is another main contributing factor that increased the risk of suicide. A report showed that Ireland was one of the countries of highest rates of mental illness in Europe, and the problem of mental illness cost over €8.2 billion a year in Ireland (Cullen, 2018). 18.5% of the population in Ireland reported that they were suffering from mental illness in 2016, and the rate of depression in both males and females were above the European average (Cullen, 2018). 28% of Irish children aged between 11 and 15 years had reported that they had experienced bullying in school, in which 14% were cyberbullying. This might contribute to mental illness and promote suicide intentions (Cullen, 2018). Moreover, females were more likely to experience mental illness and attend mental health services than males (Gavigan & McKeon, 2007). This could be explained by slower recognition of depression and lower intention to seek help for males (Gavigan & McKeon, 2007). As a result, this might be another significant factor why males have contributed to higher suicide rate than females. In addition, a large number of people who experienced mental illness would take drug or medicine such as antidepressant to reduce the pressure that might also lead to increase the risk of suicide (Departments of Public Health, 2001). Alcohol Consumption Alcohol consumption also is significantly linked with the morality of suicide. The studies showed more than half of the people who committed suicide were also related to alcohol, also more than one-third of those who drank alcohol had hurt themselves (GRIFFIN, 2014). The World Health Organisation stated that people who experienced alcohol abuse were 8 times more likely to do things unconsciously than people who didn't (WHO, 2004). Also, males seemed to drink more than female especially the younger ones (Departments of Public Health, 2001). Therefore, leading the young males aged 15–24 turned up the greatest suicide rate compared to the rest of the age groups (NSRF, 2016). Evidence showed that there was a high amount of alcohol consumption by young people usually in the weekend and public holiday as they might drink when hanging with friends or having a party (Arensman et al., 2016). Young people who drank at an earlier age might also make them drink regularly and more in the future (Departments of Public Health, 2001). Heavy drinking or alcohol abuse had a negative influence on people's mental health, especially for the young people, which increased their feeling of depression and anxiety leading to increase self-harm and suicide (Departments of Public Health, 2001). Suicide prevention Suicide thought is often a temporal thought of mind which is possible to help and provide emotional support to those people who had strong depression and anxiety, in order to reduce the risk of suicide (Health Service Executive, 2011). A focused campaign indicated that the suicide rates among 25–34 years old men decreased (Health Service Executive, 2011). WHO stated that strong partnership works together as a core element to prevent suicide (WHO, 2014). Media, school, and the government are the three major sectors which play a significant role in suicide prevention and giving support. Media The media, including the news, television, film and the internet, play a significant role in suicide prevention, especially for the younger people (Biddle et al., 2012). A study shows that teenagers are more easily affected by social media (Lin et al., 2010). The media might spread out the information to the public about the impact and the lethality rate of suicide, as well the characteristics of the suicide method especially hanging (Arensman et al., 2016). Media also takes part in promoting suicide prevention awareness, reporting suicide and providing information for assistance if someone who is thinking about committing suicide (Arensman et al., 2016). Hanging is the most common suicide method that the Irish used, especially for young people (Departments of Public Health, 2001). The suicide method that people choose is significantly related to how they perceived the information of suicide cases (Cantor & Baume, 1998). Thus, media is an important sector that linked to reducing people's cognitive availability of hanging. For example, the media should report fewer details of the suicide cases that involve hanging, such as pictures and videos (Arensman et al., 2016). The media should also follow the media guideline that avoids using profanity and sensationalism (Samaritans, 2013). School The studies showed that the suicide rate was higher in young people. Hence, the school should infuse positive mental health to their students for suicide prevention among this age group. There are different programs that can be supported by the school. For example, MindOut training is a program which was developed in 2004 by the Health Promotion Research Centre in NUI Galway and the HSE's Health Promotion and Improvement Department (HSE, 2018). This program is based on the feedback from the teacher and the young people, and elaborated by the researchers. It has been proven to improve young people's overall mental health and wellbeing, strengthen their emotional competence, and the ability to cope with their own personal difficulties (HSE, 2018). Teachers and parents are the most important stakeholders for the school to promote these approaches (HSE, 2018). In addition, the school should educate their students on how drinking alcohol and taking drug might impact their mental health and increase the feeling of depression (Arensman et al., 2016). Moreover, they should as well explain how drugs and alcohol contribute to suicide intentions (Arensman et al., 2016). Government The Government of Ireland proposed to decrease the mortality rate of suicide and improve national overall mental health and wellbeing by several approaches. These include providing society better suicide awareness, giving support to the communities, improving safety, access and quality of the service, better research and use target approaches to identify the specified priority group of suicide, etc. (HSE, 2017). The government also aimed to reduce the overall suicide rate and self-harm rate of the whole population by the project "Connecting of life" (Department of Health, 2015). Connecting for life, which is the national office's project, aimed to reduce the suicide rate in 2015-2020 (Department of Health, 2015). This project provides free and evidence-based suicide and self-harm training which aimed to increase public awareness and governmental support for suicide prevention. In 2017, over 12000 Irish people have completed programs such as Applied Suicide Intervention Skills Training (ASIST) (Department of Health, 2015). Currently, all 17 local action plans are placed for supporting suicide prevention (Department of Health, 2015). The National Office had funded more than €11.9 million in 2017, and approximately 60% of the fund was used in agencies and front-line services for meeting the target of Connecting for life and researching (Department of Health, 2015). References Arensman, Ella & Bennardi, Marco & Larkin, Celine & Wall, Amanda & Mcauliffe, Carmel & McCarthy, Jacklyn & Williamson, Eileen & J. Perry, Ivan. (2016). Suicide among Young People and Adults in Ireland: Method Characteristics, Toxicological Analysis, and Substance Abuse Histories Compared. PLOS ONE. 11. e0166881. 10.1371/journal.pone.0166881. Biddle, L., Gunnell, D., Owen-Smith, A., Potokar, J., Longson, D., Hawton, K., ... Donovan, J. (2012). Information sources used by the suicidal to inform choice of method. Journal of Affective Disorders, 136(3), 702–709. Burke, S., & McKeon, P. (2007). Suicide and the reluctance of young men to use mental health services. Irish Journal of Psychological Medicine, 24(2), 67-70. doi:10.1017/S0790966700010260 Central Statistics Office. (2013). Vital Statistics Fourth Quarter and Yearly Summary Child Safety Europe. (2014). What are European countries doing to prevent intentional injury to children? Cullen, P. (2018). Ireland has one of the highest rates of mental health illness in Europe, report finds. THE IRISH TIMES Department of Health. (2015). Connecting for life : Ireland's national strategy to reduce suicide 2015-2020. Ireland, Dublin : Department of Health Departments of Public Health. (2001). Suicide in Ireland. Departments of Public Health. eurostat. (2019). Unemployment by sex and age - monthly average. GRIFFIN, E., ARENSMAN, E., PAUL CORCORAN, P., CHRISTINA B DILLON, C., WILLIAMSON, E., PERRY, I. (2014). NATIONAL SELF-HARM REGISTRY IRELAND ANNUAL REPORT 2014, The National Suicide Research Foundation. Lin, Jin-Jia & Chang, Shu-Sen & Lu, Tsung-Hsueh. (2010). The leading methods of suicide in Taiwan, 2002-2008. BMC public health. 10. 480. 10.1186/1471-2458-10-480. Mental Health First Aid (2016) HELPING SOMEONE WITH MENTAL HEALTH PROBLEMS AND FINANCIAL DIFFICULTIES: GUIDELINES FOR THE SUPPORT PERSON OECD/European Union. (2018). “Promoting mental health in Europe: Why and how?”, in Health at a Glance: Europe 2018: State of Health in the EU Cycle, OECD Publishing, Paris/European Union, Brussels. doi: https://doi.org/10.1787/health_glance_eur-2018-4-en Orla, R. (2018). Men account for eight in 10 suicides in Ireland. TheJournal.ie Preti, A., & Miotto, P. (1999). Suicide and unemployment in Italy, 1982-1994. Journal of epidemiology and community health, 53(11), 694–701. doi:10.1136/jech.53.11.694 Richardson, N., Clarke, N., & Fowler, C. (2013). A report on the all-Ireland young men and suicide project. Carlow: Men's Health Forum in Ireland. Samaritans. (2013) MEDIA GUIDELINES for Reporting Suicide. Samaritans. The Health Service Executive. (2011). Suicide. The Health Service Executive. The Health Service Executive. (2017). National Office for Suicide Prevention Annual Report 2017. The Health Service Executive. The Health Service Executive. (2018). Launch of newly revised MindOut Programmes for schools. The Health Service Executive. The National Suicide Research Foundation. (2016). Suicide. The National Suicide Research Foundation. World Health Organisation. (2012). Programmes and Projects, Mental Health, Suicide Prevention, Country Reports and Charts. World Health Organization. World Health Organisation. (2004). Global Status Report on Alcohol. World Health Organization. World Health Organization. (2014). Preventing suicide: a global imperative. World Health Organization. Category:Suicide Category:Ireland
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Witt vector In mathematics, a Witt vector is an infinite sequence of elements of a commutative ring. Ernst Witt showed how to put a ring structure on the set of Witt vectors, in such a way that the ring of Witt vectors over the finite field of order p is the ring of p-adic integers. History In the 19th century, Ernst Eduard Kummer studied cyclic extensions of fields as part of his work on Fermat's Last Theorem. This led to the subject now known as Kummer theory. Let k be a field containing a primitive nth root of unity. Kummer theory classifies degree n cyclic field extensions K of k. Such fields are in bijection with order n cyclic groups , where corresponds to . But suppose that k has characteristic p. The problem of studying degree p extensions of k, or more generally degree pn extensions, may appear superficially similar to Kummer theory. However, in this situation, k cannot contain a primitive pth root of unity. If x is a pth root of unity in k, then it satisfies . Because raising to the pth power is the Frobenius homomorphism, this equation may be rewritten as , and therefore . Consequently Kummer theory is never applicable to extensions whose degree is divisible by the characteristic. The case where the characteristic divides the degree is now called Artin–Schreier theory because the first progress was made by Artin and Schreier. Their initial motivation was the Artin–Schreier theorem, which characterizes the real closed fields as those whose absolute Galois group has order two. This inspired them to ask what other fields had finite absolute Galois groups. In the midst of proving that no other such fields exist, they proved that degree p extensions of a field k of characteristic p were the same as splitting fields of Artin–Schreier polynomials. These are by definition of the form . By repeating their construction, they described degree p2 extensions. Abraham Adrian Albert used this idea to describe degree pn extensions. Each repetition entailed complicated algebraic conditions to ensure that the field extension was normal. Schmid generalized further to non-commutative cyclic algebras of degree pn. In the process of doing so, certain polynomials related to addition of p-adic integers appeared. Witt seized on these polynomials. By using them systematically, he was able to give simple and unified constructions of degree pn field extensions and cyclic algebras. Specifically, he introduced a ring now called Wn(k), the ring of n-truncated p-typical Witt vectors. This ring has k as a quotient, and it comes with an operator F which is called the Frobenius operator because it reduces to the Frobenius operator on k. Witt observes that the degree pn analog of Artin–Schreier polynomials is where . To complete the analogy with Kummer theory, define to be the operator . Then the degree pn extensions of k are in bijective correspondence with cyclic subgroups of order pn, where corresponds to the field . Motivation Any -adic integer (an element of , not to be confused with ) can be written as a power series , where the 's are usually taken from the integer interval . It is hard to provide an algebraic expression for addition and multiplication using this representation, as one faces the problem of carrying between digits. However, taking representative coefficients is only one of many choices, and Hensel himself (the creator of p-adic numbers) suggested the roots of unity in the field as representatives. These representatives are therefore the number together with the roots of unity; that is, the solutions of in , so that . This choice extends naturally to ring extensions of in which the residue field is enlarged to with , some power of . Indeed, it is these fields (the fields of fractions of the rings) that motivated Hensel's choice. Now the representatives are the solutions in the field to . Call the field , with an appropriate primitive root of unity (over ). The representatives are then and for . Since these representatives form a multiplicative set they can be thought of as characters. Some thirty years after Hensel's works Teichmüller studied these characters, which now bear his name, and this led him to a characterisation of the structure of the whole field in terms of the residue field. These Teichmüller representatives can be identified with the elements of the finite field of order by taking residues modulo in , and elements of are taken to their representatives by the Teichmüller character . This operation identifies the set of integers in with infinite sequences of elements of . Taking those representatives the expressions for addition and multiplication can be written in closed form. We now have the following problem (stated for the simplest case: ): given two infinite sequences of elements of describe their sum and product as -adic integers explicitly. This problem was solved by Witt using Witt vectors. Detailed motivational sketch We derive the ring of -adic integers from the finite field using a construction which naturally generalizes to the Witt vector construction. The ring of -adic integers can be understood as the projective limit of Specifically, it consists of the sequences with such that for That is, each successive element of the sequence is equal to the previous elements modulo a lower power of p; this is the inverse limit of the projections . The elements of can be expanded as (formal) power series in where are usually taken from the integer interval Of course, this power series usually will not converge in using the standard metric on the reals, but it will converge in with the p-adic metric. We will sketch a method of defining ring operations for such power series. Letting be denoted by , one might consider the following definition for addition: and one could make a similar definition for multiplication. However, this is not a closed formula, since the new coefficients are not in the allowed set There is a better coefficient subset of which does yield closed formulas, the Teichmuller representatives: zero together with the roots of unity. They can be explicitly calculated (in terms of the original coefficient representatives ) as roots of through Hensel lifting, the p-adic version of Newton's method. For example, in to calculate the representative of , one starts by finding the unique solution of in with ; one gets . Repeat this in , with the conditions and gives and so on; the resulting Teichmüller representative is the sequence The existence of a lift in each step is guaranteed by the greatest common divisor in every This algorithm shows that for every , there is exactly one Teichmuller representative with , which we denote Indeed, this defines the Teichmüller character satisfying if we denote Note that is not additive, as the sum need not be a representative. Despite this, if in then in Because of this one-to-one correspondence given by , one can expand every -adic integer as a power series in with coefficients taken from the Teichmüller representatives. An explicit algorithm can be given, as follows. Write the Teichmüller representative as Then, if one has some arbitrary p-adic integer of the form one takes the difference leaving a value divisible by . Hence, . The process is then repeated, subtracting and proceed likewise. This yields a sequence of congruences So that and implies: for Hence we have a power series for each residue of x modulo powers of p, but with coefficients in the Teichmüller representatives rather than . It is clear that since for all as so the difference tends to 0 with respect to the p-adic metric. The resulting coefficients will typically differ from the 's modulo , except the first one. The Teichmuller coefficients have the key additional property that which is missing for the numbers in . This can be used to describe addition, as follows. Since the Teichmüller character is not additive, is not true in . But it holds in as the first congruence implies. In particular, and thus Since the binomial coefficient is divisible by , this gives This completely determines by the lift. Moreover, the congruence modulo indicates that the calculation can actually be done in satisfying the basic aim of defining a simple additive structure. For this step is already very cumbersome. Write Just as for a single th power is not enough: one must take However, is not in general divisible by but it is divisible when in which case combined with similar monomials in will make a multiple of . At this step, it becomes clear that one is actually working with addition of the form This motivates the definition of Witt vectors. Construction of Witt rings Fix a prime number p. A Witt vector over a commutative ring R is a sequence: of elements of R. Define the Witt polynomials by and in general The are called the ghost components of the Witt vector , and are usually denoted by The ghost components can be thought of as an alternative coordinate system for the R-module of sequences. The ring of Witt vectors is defined by componentwise addition and multiplication of the ghost components. That is, that there is a unique way to make the set of Witt vectors over any commutative ring R into a ring such that: the sum and product are given by polynomials with integral coefficients that do not depend on R, and projection to each ghost component is a ring homomorphism from the Witt vectors over R, to R. In other words, and are given by polynomials with integral coefficients that do not depend on R, and and . The first few polynomials giving the sum and product of Witt vectors can be written down explicitly. For example, . These are to be understood as shortcuts for the actual formulas. If for example the ring R has characteristic p, the division by p in the first formula above, the one by that would appear in the next component and so forth, do not make sense. However, if the p-power of the sum is developed, the terms are cancelled with the previous ones and the remaining ones are simplified by p, no division by p remains and the formula makes sense. The same consideration applies to the ensuing components. Examples The Witt ring of any commutative ring R in which p is invertible is just isomorphic to (the product of a countable number of copies of R). In fact the Witt polynomials always give a homomorphism from the ring of Witt vectors to , and if p is invertible this homomorphism is an isomorphism. The Witt ring of the finite field of order p is the ring of p-adic integers written in terms of the Teichmuller representatives, as demonstrated above. The Witt ring of a finite field of order pn is the unramified extension of degree n of the ring of p-adic integers. Universal Witt vectors The Witt polynomials for different primes p are special cases of universal Witt polynomials, which can be used to form a universal Witt ring (not depending on a choice of prime p). Define the universal Witt polynomials Wn for n ≥ 1 by and in general Again, is called the vector of ghost components of the Witt vector , and is usually denoted by . We can use these polynomials to define the ring of universal Witt vectors over any commutative ring R in much the same way as above (so the universal Witt polynomials are all homomorphisms to the ring R). Generating Functions Witt also provided another approach using generating functions. Definition Let be a Witt vector and define For let denote the collection of subsets of whose elements add up to . Then We can get the ghost components by taking the logarithmic derivative: Sum Now we can see if . So that if are the respective coefficients in the power series . Then Since is a polynomial in and likewise for , we can show by induction that is a polynomial in Product If we set then But . Now 3-tuples with are in bijection with 3-tuples with , via ( is the least common multiple), our series becomes So that where 's are polynomials of So by similar induction, suppose then can be solved as polynomials of Ring schemes The map taking a commutative ring R to the ring of Witt vectors over R (for a fixed prime p) is a functor from commutative rings to commutative rings, and is also representable, so it can be thought of as a ring scheme, called the Witt scheme, over The Witt scheme can be canonically identified with the spectrum of the ring of symmetric functions. Similarly, the rings of truncated Witt vectors, and the rings of universal Witt vectors correspond to ring schemes, called the truncated Witt schemes and the universal Witt scheme. Moreover, the functor taking the commutative ring to the set is represented by the affine space , and the ring structure on makes into a ring scheme denoted . From the construction of truncated Witt vectors, it follows that their associated ring scheme is the scheme with the unique ring structure such that the morphism given by the Witt polynomials is a morphism of ring schemes. Commutative unipotent algebraic groups Over an algebraically closed field of characteristic 0, any unipotent abelian connected algebraic group is isomorphic to a product of copies of the additive group . The analogue of this for fields of characteristic p is false: the truncated Witt schemes are counterexamples. (We make them into algebraic groups by forgetting the multiplication and just using the additive structure.) However, these are essentially the only counterexamples: over an algebraically closed field of characteristic p, any unipotent abelian connected algebraic group is isogenous to a product of truncated Witt group schemes. See also Formal group Artin–Hasse exponential Necklace ring References , section II.6 Category:Ring theory Category:Algebraic groups Category:Combinatorics on words
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Q: exact definition of open sets What is the exact definition of open sets? I know both definitions of open sets with respect to metric space and topological space. but what is most general definition that covers the both. A: Let $X$ be a set. An open set is an element of a collection $\mathcal{T}$ (whose elements are subsets of $X$), called a topology, which satisfies three conditions. $\varnothing$ and $X$ are elements of $\mathcal{T}$. For any subcollection $\mathcal{S}$ of $\mathcal{T}$, the union $\bigcup\mathcal{S}$ is an element of $\mathcal{T}$. For any finite subcollection $\mathcal{S}$ of $\mathcal{T}$, the intersection $\bigcap\mathcal{S}$ is an element of $\mathcal{T}$. Let $(M,\rho)$ be a metric space. Then the metric topology $\mathcal{T}_{\rho}$ induced by the metric $\rho$ is the collection of sets of the form $\bigcup\mathcal{B}$, where $\mathcal{B}$ is any collection (possibly empty) of open balls. Here an open ball is a set of the form $\{x\in M:\rho(x_0,x)<r_0\}$ for fixed $x_0\in M$ and for fixed positive real number $r_0$. A: There is no definition of what an open set is. There is a definition of what a Topology, and each Topology will have a class of sets that are called open but these sets can pretty much be anything we want so far as the class of sets obey certain rules of inclusion. A metric space is a type of topological space and the definition of an open set in a metric space is such that the class of all open sets obeys the rules of inclusion required for the metric space to be considered a topology. So the definition of a Topology is the most general definition. But every topology will have its own classification of what open sets are. These classifications of sets must obey certain rules but the actual open sets themselves need not have any consistent properties. .... More precisely if a have a universal set $X$ then ANY $T \subset P(X)$ (any class of subsets of $X$) can be called the class of all "open" sets so long as the following apply: $X$ and $\emptyset$ are elements of $T$. The union of sets in $T$ will itself be in $T$ Any finite intersection of sets in $T$ will itself be in $T$ As long as those rules are obeyed any set can be considered open. If we have a metric space $X$ and we define that if a set $A\subset X$ is such: that for every point $x\in A$ there will be an open ball $B_r(x)$ around $x$ so that $B_r(x) \subset A$; we call such a set PEN-Oay. Now $X$ is PEN-Oay because everything including all open balls are subsets of it. And $\emptyset$ is PEN-Oay vacuously because it has no points (as every point can be said to have any property). And we can prove but I will not that any union (even infinite unions) of PEN-Oay sets are PEN-Oay. And we can prove any finite intersection of PEN-Oay sets are PEN-Oay. So if being PEN-Oay satisfies all three conditions for the class of all PEN-Oay sets to be considered a class of all "open" sets. So we can say the metric space is a Topology so that $T = \{$ all "open" set$\} = \{$ all PEN-Oay sets$\}$.
3.625
4
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Following a meal, increased blood glucose levels stimulate insulin release from the pancreas to act throughout the body to lower blood glucose levels. Important sites of action of insulin on glucose metabolism include facilitation of glucose uptake into skeletal muscle and adipocytes, and an increase of glycogen storage in the liver. Skeletal muscle and adipocytes is responsible for insulin-mediated glucose uptake and utilization in the fed state, making them very important sites for glucose metabolism. Diabetes comprises two distinct diseases, viz. type 1 (or insulin-dependent diabetes) and type 2 (insulin-independent diabetes), both of which involve the malfunction of glucose homeostasis. Type 2 diabetes affects more than 350 million people in the world and the number is rising rapidly. Complications of diabetes include severe cardiovascular problems, kidney failure, peripheral neuropathy, blindness and even loss of limbs and death in the later stages of the disease. Type 2 diabetes is characterized by insulin resistance in skeletal muscle and adipose tissue (fat), and at present there is no definitive treatment. Most treatments used today are focused on treating dysfunctional insulin signaling or inhibiting glucose output from the liver and many of those treatments have several drawbacks and side effects. There is thus a great interest in identifying novel insulin-independent ways to treat different form of metabolic orders connected with dysregulation of glucose uptake such as type 2 diabetes. In type 2 diabetes the insulin-signaling pathway is blunted in peripheral tissues such as fat and skeletal muscle. Methods for treating type 2 diabetes typically include lifestyle changes, as well as the administration of insulin or oral medications to help the body with the glucose homeostasis. People with type 2 diabetes in the later stages of the disease develop “beta-cell failure” or the inability of the pancreas to release insulin in response to high blood glucose levels. In the later stages of the disease patients often require insulin injections, in combination with oral medications, to manage their diabetes. In type 2 diabetes the insulin-signaling pathway is blunted in peripheral tissues and most common drugs have side effects including the said down regulation or desensitization of the insulin pathway and/or the promotion of fat incorporation in fat, liver and skeletal muscle, furthermore increased stimulation of proliferation of certain cells and a higher risk of promoting cancer. There is thus a great interest in identifying novel ways to treat metabolic diseases including type 2 diabetes that do not include these side-effects. The molecular understanding of the signaling pathway below the insulin receptor has been a very hard problem to solve and has been occupying a great number of researchers since the discovery of insulin. In short, control of glucose uptake by insulin involves activation of the insulin receptor (IR), insulin receptor substrate (IRS), phosphoinositide 3-kinase (PI3K) and thus stimulation of phosphatidylinositol (3,4,5)-triphosphate (PIP3), mammalian target of rapamycin also called mechanistic target of rapamycin (mTOR), Akt/PKB (Akt) and TBCID4 (AS160), leading to translocation of glucose transporter 4 (GLUT4). Akt activation is considered necessary for GLUT4 translocation. Akt has multiple act ions and regulates cellular metabolism and survival. Akt can promote cell survival both directly and indirectly. Akt can promote proliferation and differentiation and has impact on the cell cycle and migration of cells. Akt can influence transcription and translation. Akt has been implicated in angiogenesis and tumor growth. Thus Akt promotes changes in cells and tissues that can lead to cancer and other pathophysiological effects, such as obesity and negative effects on insulin signaling. It would thus be desirable to be able to increase glucose uptake without stimulating Akt to circumvent these side-effects. Another important protein involved in the insulin-signaling pathway is mTOR. mTOR is regulated by several upstream pathways involved in energy uptake of the cell. mTOR is a complex that exists in two complexes: mTOR complex-1 (mTORC1), which includes the protein raptor, and mTOR complex-2 (mTORC2), which includes the protein rictor. PI3K has a key function upstream of mTOR in the insulin pathway by generating polyphosphoinositides in the plasma membrane, which function as a docking site for Akt. Thereby Akt is brought close to its activating kinases, PDK-1, which phosphorylates Akt on Thr308, and mTORC2, which phosphorylates Akt on Ser473 (Rowland, Fazakerley & James 2011). Insulin and catecholamines are released in the body in response to quite different stimuli. Whereas insulin is released in response to the rise in blood sugar levels after a meal, epinephrine (also referred to as adrenaline) and norepinephrine (also referred to as noradrenaline) are released due to various internal and external stimuli, such as exercise, emotions and stress but also homeostatic tissue regulation. Insulin is an anabolic hormone that stimulates many processes involved in growth including glucose uptake, glycogen and triglyceride formation whereas catecholamines are mainly catabolic. Although insulin and catecholamines normally have antagonistic effects, it has been shown previously that they have similar actions in skeletal muscle on glucose uptake (Nevzorova et al. 2006). It is likely that catecholamines stimulate glucose uptake via adrenergic receptors to supply muscle cells with an energy substrate. Thus, it is likely that in mammals, including humans, the adrenergic and insulin systems can work independently to provide for the energy need of skeletal muscle during different situations. Since insulin stimulates many anabolic processes including a number of unwanted side effects it would be beneficial to be able to stimulate glucose uptake through the newly found adrenergic signaling pathway, which is catabolic and does not include many of the unwanted processes. It is known in the field of the art that adrenergic receptors are prototypic models for the study of G protein-coupled receptors (GPCRs) and their signaling (Santulli, laccarino 2013, Drake, Shenoy & Leficowitz 2006). There are three different classes of ARs, with distinct expression patterns and pharmacological profiles: α1-, α2- and β-ARs. The α1-ARs comprise the α1A, α1B and α1D while α2-ARs are divided into α2A, α2B- and α2C. The β-ARs are also divided into the subtypes β1, β2, and β3, of which β2-AR is the major isoform in skeletal muscle cells (Watson-Wright, Wilkinson 1986, Liggett, Shah & Cryer 1988). Adrenergic receptors are G protein coupled and signal through second messengers such as cAMP and phospholipase C and are thus suited as prototypical models for most classes of GPCRs. Glucose uptake in cells is mainly considered to be through facilitative glucose transporters (GLUT). GLUTs are transporter proteins mediating transport of glucose and/or fructose over the plasma membrane down the concentration gradient. There are fourteen known members of the GLUT family, named GLUT1-14, divided into three classes (Class I, Class II and Class III) dependent on their substrate specificity and tissue expression. GLUT1 and GLUT4 are the most intensively studied isoforms and, together with GLUT2 and GLUT3, belong to Class I which mainly transports glucose (in contrast to Class II that also transports fructose). GLUT1 is ubiquitously expressed and is responsible for basal glucose transport. GLUT4 is only expressed in peripheral tissues such as skeletal muscle, cardiac muscle and adipose tissues. GLUT4 has also been reported to be expressed in e.g. brain, kidney, and liver. GLUT4 is the major isoform involved in insulin stimulated glucose uptake. To treat a condition involving a dysregulation of glucose homeostasis or glucose uptake in a mammal, it would be very advantageous to be able to activate certain GLUTs. For example for diseases such as type 2 diabetes it is vital to activate GLUT4 translocation to the plasma membrane and thus glucose uptake. Regulation of GLUT1 translocation or intrinsic activity has been suggested to occur in several tissues including erythrocytes depending on ATP-levels (Hebert, Carruthers 1986). It has also been indicated in HEK-cells (Palmada et al. 2006), 3T3-L1 (Harrison et al. 1992) and clone-9 cells (Barnes et al. 2002). Impaired GLUT translocation, of in particular GLUT8, has been reported as involved in both male and female infertility (Gawlik et al. 2008, Carayannopoulos et al. 2000). The mechanism whereby insulin signaling increases glucose uptake is mainly via GLUT4-translocation from intracellular storage to the plasma membrane (Rodnick et al. 1992). After longer insulin stimulation also GLUT1-content is increased due to increased transcription (Taha et al. 1995). Glucose uptake in type 2 diabetes is associated with defects in PI3K activity, insulin receptor tyrosine, IRS and Akt phosphorylation, resulting in impairment of GLUT4 translocation to the plasma membrane. Impaired GLUT translocation also plays a role in muscle wasting. Furthermore, GLUT translocation plays a role in feeding behavior. Mice lacking GLUT4 develop problems with lipid and glucose homeostasis leading to changes in feeding behavior. Decreased concentrations of GLUT1 and GLUT3 have also been shown in the brains of patients with Alzheimer's disease (Simpson et al 2008). Also in a review article of Shah K, et al. (Shah, Desilva & Abbruscato 2012) the role of glucose transporters in brain disease, diabetes and Alzheimer's disease is discussed.
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Digital image processing, such as compression, transmission, browsing and communications is common in the art. Typically early methods of digital image transmission and storage used so-called Pulse Code Modulation (PCM). More recent systems use more complicated digital compression techniques. Digital compression techniques according to the state of the art are based on transform coding. One such compression technique is the JPEG format as standardized by the Joint Photographic Experts Group according to the standards ITU-T T.81, ISO/IEC IS 10918-land ITU-T T.84, see inter alia “The JPEG Handbook”, by W. Pennebaker, J. Mitchell, Van Nostrand Reinhold, 1993. It is also common to post-process compressed images. Post-processing may involve applying filters, changing the image format, etc. Post-processing may also involve scaling the compressed image to fit a small screen, and then zooming and panning the scaled image. One product for post-processing compressed images is the PhotoShop software suite provided by Adobe Systems Incorporated of USA.
3.265625
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Equine infectious anemia found in horse A pony recently obtained by an equine rescue group from a sale barn in Pennsylvania and brought to a stable on a New Jersey premises has been confirmed positive for Equine Infectious Anemia (EIA). Officials in Pennsylvania are investigating the source of the infection. The pony has been euthanized. Equine Infectious Anemia (EIA), also known as swamp fever, is an infectious, viral disease that infects all equidae (horses, donkeys, zebras, etc.) It is not infectious to humans. There is no effective treatment or approved vaccine available for Equine Infectious Anemia. The disease is spread via blood-to-blood transmission, not close proximity or casual contact. EIA is usually transmitted from horse to horse by large biting insects such as horseflies and deerflies. The bites from these flies stimulate defensive movement by the horse, which often results in an interruption of the flies' blood feeding. When interrupted, flies are motivated to complete feeding as soon as possible. They then attack the same or a second host and feed to complete their meal. Any infective material from the blood of the first host that is present on the mouthparts of the flies can be transmitted to the second host. Blood transfusions, unsterilized or contaminated needles and equipment contaminated with blood from an infected horse can also spread the virus. Depending on an individual horse's immune system and the severity of its reaction, clinical signs of EIA can range dramatically. While some infected with EIA show no signs of illness, others display fever, weight loss, icterus (yellowing of body tissues), anemia, swelling of the limbs, weakness, rejection of feed, and/or sudden death. To minimize disease transmission, all equidae should be tested for EIA before being brought onto a new premises. The animal should be isolated and observed for 45 to 60 days, then retested before being introduced to the herd. New Jersey law requires all imported equidae to have a negative official test for EIA within the past 12 months. All equidae traveling on New Jersey roads must have a negative EIA test a maximum of 24 months prior to such travel, and any equidae that change ownership must be tested a maximum of 90 days prior to such a change in ownership. Equidae younger than six months and accompanied by a dam (female parent) that has a negative official test within the past 12 months are exempt from EIA testing. For further information about EIA or information about EIA testing performed at the NJDA-Division of Animal Health Diagnostic Laboratory, please contact Dr. Nancy Halpern at 609-292-3965 or via email at Nancy.Halpern@ag.state.nj.us.
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Soil Compaction can be cause by many sources. Farming equipment, such as trucks and tractors, can lead to fragipan. Earth moving equipment can also cause compaction. Pastures can even be compacted by animals when field are wet (McMahon 147). That means even lawn mowers and people can cause compaction in their own lawn & garden. Especially when the soil is wet. These compacted soils have a higher Bulk Density. As the Bulk Density goes up, the pore space goes down. Pore space is a needed part in the growth of any plant; grass, roses, corn, tomatoes, flowers. Remember, Field Capacity is the point where there is an equal amount or distribution of water and air in the soil profile. Plants need both air and water to survive. Compacted soils do not allow water, air or roots to penetrate easily. Water, air and roots are necessary for a healthy enviroment to grow plants and sustain the ecosystem for other organisms (Utah.gov).
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Q: What is the conjugate variable of angular momentum? We know that for Heisenberg uncertainty principle, position and momentum are conjugates, energy and time are conjugates. Like wise what is the conjugate variable for angular momentum? Is it orientation along with something? Or anything else? P.Q:-Another observation, the unit of Angular momentum already is kg*m^2/s, which is supposed to be the unit of uncertainty. So the conjugate variable must be unit less A: From Wikipedia, conjugate variables have a general definition: In classical physics, the derivatives of action are conjugate variables to the quantity with respect to which one is differentiating. In quantum mechanics, these same pairs of variables are related by the Heisenberg uncertainty principle. In the same way that the conjugate of linear momentum is position ($x$), the conjugate of angular momentum is "angular position", a.k.a. orientation. You can find a list of other conjugate pairs here. As for the units of orientation, indeed, radians are dimensionless: Although the radian is a unit of measure, it is a dimensionless quantity. This can be seen from the definition given earlier: the angle subtended at the centre of a circle, measured in radians, is equal to the ratio of the length of the enclosed arc to the length of the circle's radius. Since the units of measurement cancel, this ratio is dimensionless.
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What does Hemoglobin Mean? Hemoglobin is the protein molecule in the red blood cells that are responsible for carrying the oxygen from the lungs to your bodies tissue and returns the carbon dioxide waste from the tissue to the lungs.
3.328125
3
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Infectious diseases have wrecked continents, treatment-resistant superbugs are increasing, and social stigma inhibits treatment of crippling psychiatric conditions. At times, the state of international health might appear hopeless and worrying. But in reality, a variety of advances, from drug development to disease tracking, are helping people live longer at a scale that was formerly unthinkable. In the past decade, one technology, in specific, has had an outsized impact on global health: the smart phone. By transforming the way we interact with each other, even the simplest cell phone has enabled epidemiologists to track disease outbreaks with higher accuracy than in the past. Understanding how a disease spreads and where it spreads out is crucial if scientists are to find a way to fight and, hopefully, beat it. Smart phones do even more to improve global health. The hardware has democratized health technologies that used to be too costly or too physically far for many people to access. With smart phones, doctors can perform sophisticated medical tests or procedures without setting foot in a laboratory; patients can better comprehend their own health and control their info. Here are 5 ways that smartphone or cell phones have had a fundamental impact on worldwide health. Emergency Care In case of a medical emergency, dialing 911 is the most reliable way to get assistance in a rush in the US (it’s 999 in the UK). But for folks who live in rural areas, particularly in underdeveloped countries, rapid emergency care is far from a guarantee. The app ‘MUrgency‘ promises to streamline that procedure. Depending on the kind of emergency, it can link patients to ambulances faster, or even provide users with a qualified nurse to help them right at home. The app is intended to compensate when governments cannot do the job. Depending on where you live in the United States, it can take between 6 and 35 minutes for an ambulance to show up in a medical emergency. MUrgency is designed to offer timely emergency care, whether a patient resides in a rural location or an urban city. This is only possible thanks to the ubiquity of smart phones. The service was launched in 2016 in Punjab, India with a network of 36 hospital emergency rooms, over 40 ambulances and 350 physicians. It won 1st Prize in Health & Wearables at the 2016 SXSW Festival in Austin, Texas. Now, patients can access responder services in Punjab; those services are expected to become available in other cities such as Dubai by the end of 2018. Screening for Pancreatic Cancer To detect pancreatic cancer, all you have to do is take a selfie. That’s possible thanks to scientists at the University of Washington who developed a smart phone app that can screen for pancreatic cancer. The cutting-edge technology utilizes computer vision algorithms and artificial intelligence to identify jaundice in the whites of patients’ eyes. Jaundice is caused by high levels of bilirubin, a yellow substance that can indicate the early stages of pancreatic cancer. In a research study of 70 individuals, the app had a success rate of about 90 percent, about the same precision as the blood tests that are the existing standard. “The hope is that if people can do this simple test once a month — in the privacy of their own houses — some might catch the disease early enough to undergo treatment that could save their lives,” Alex Mariakakis, a doctoral student at the Paul G. Allen School of Computer Science & Engineering told the University of Washington News. Detecting Pathogens In The Blood Physicians use test patients’ blood to look for a number of elements of health, from finding cholesterol levels to diagnosing rare tropical diseases. Most blood tests need a lab for analysis, however sophisticated laboratories and equipment are not always readily available, depending on where the patient is located. For remote clinics, dispatching the samples and awaiting the results can take days or weeks, and during this time, a patient obviously is not getting treatment. To accelerate that procedure, scientists from 2 universities have miniaturized a blood lab into a handheld gadget that works with a smartphone. A single drop of blood is all it takes to check for dengue, Zika, and other infectious diseases. The gadget itself (without the smart phone) is just the size of a visiting card. Grooves in the chip suck in small amounts of blood that are illuminated by the phone’s LED. A group of sensors analyze how light traves through the blood, which the system compares with the results of tests found to be positive. The whole procedure takes 10 minutes. “Labs-on-a-chip” are inexpensive and fast, and diagnostics can be performed in practically any environment. The scientists hope their gadget can detect a lot more pathogens in the future. A similar lab-on-a-chip, developed by researchers at the Fraunhofer Institute for Cell Therapy & Immunology in Leipzig, Germany, can identify E. coli and salmonella pathogens in the blood. Similarly, scientists at Columbia University have developed a smart phone dongle that can identify syphilis and HIV in just 15 minutes “Coupling microfluidics with recent advances in electronics can make certain laboratory-based diagnostics accessible to almost any population with access to smart phones. This kind of capability can transform how health care services are delivered around the globe,” Samuel Sia, an associate professor of biomedical engineering at Columbia University, stated in a 2015 article published on the university’s website. Tracking the Spread of Disease Epidemiology is a deceptively complex field. Researchers have to pinpoint the origin and reason for an outbreak, often as it continues to spread out. Collecting information can be difficult in rural areas; infrastructure (or lcack of it) can restrict communication. Even if researchers have a good understanding of the signs of the disease and the way it is transmitted to human beings, they might still have a hard time to keep track of those who are contaminated. Mobile phones have changed that. Now scientists are able to track the malaria parasite across Kenya. By overlaying maps of the prevalence of malaria over call or text data that tracked individual callers’ movements, researchers at the Harvard School of Public Health have assisted authorities strategically deploy mosquito nets, control task forces, and medications in Nairobi and surrounding locations to prevent malaria from spreading out there. Healthcare workers themselves communicate a lot more efficiently through short messaging services (SMS), according to a 2010 review. In South Africa, SMS allowed HIV-positive patients to notify or trace partners, track physician’s appointments, and utilize prevention methods. Foster Communication Smartphones have also assisted health care professionals share expertise, collected data, and other insights, no matter where they live. Social networks such as doximity enable over half a million physicians to connect online to share details and to peer-review each other’s work while still keeping identifying patient information private. It likewise helps medical professionals streamline their workload — physicians can now gain access to patient records directly on the app, or they can even call patients seamlessly. The patient can opt to either log in online, utilizing their email and password, or call their health care expert directly through the app. As chronic diseases such as hypertension and diabetes become more widespread, smart phones allow physicians to remotely monitor patients’ health. Health care professionals can provide guidance based on information that the patient collects.
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Goths The Goths (; ) were an early Germanic people who played a major role in the fall of the Western Roman Empire and the emergence of Medieval Europe. They were first definitely reported by Graeco-Roman authors in the third century, living north of the Danube in what is now Ukraine, Moldova and Romania. Later, many moved into the Roman empire, or settled west of the Carpathians near what is now Hungary. A people called the Gutones—possibly early Goths—are documented living near the lower Vistula in the 1st century AD, where they are associated with the archaeological Wielbark culture. In his book Getica, the Gothic historian Jordanes claimed that the Goths originated in southern Scandinavia more than 1000 years earlier, but his reliability is disputed. The Wielbark culture expanded southwards towards the Black Sea, where by the late 3rd century AD it contributed to the formation of the Chernyakhov culture, which is associated with the Goths who were in frequent conflict and contact with the Roman Empire. By the 4th century AD at the latest, several groups were distinguishable, among whom the Thervingi and Greuthungi were the most powerful. During this time, Ulfilas began the conversion of Goths to Arianism. In the late 4th century, the lands of the Goths were invaded from the east by the Huns. In the aftermath of this event, several groups of Goths fell under Hunnic rule, while others migrated into the Roman Empire, where they inflicted a devastating defeat upon the Romans at the Battle of Adrianople in 378. These Goths became known as the Visigoths, and under their king Alaric I they began a long migration, which culminated in them establishing a Visigothic Kingdom in Spain at Toledo. Meanwhile, Goths under Hunnic rule regained their freedom in the 5th century AD, and eventually became known as the Ostrogoths. Under their king Theodoric the Great, these Goths established an Ostrogothic Kingdom in Italy at Ravenna. The Ostrogothic Kingdom was destroyed by the Eastern Roman Empire in the 6th century AD, while the Visigothic Kingdom was conquered by the Umayyad Caliphate in the early 8th century AD. Remnants of Gothic communities in the Crimea, known as the Crimean Goths, lingered on for several centuries, although Goths would eventually cease to exist as a distinct people. Name The name "Goths" means "men" or "the people". In the Gothic language of the Ostrogothic Kingdom in Italy, the Goths were called the *Gut-þiuda "Gothic people" (attested as dative singular Gut-þiudai). The simplex variant of this name, *Gutans, or possibly *Gutôs, is inferred from a presumed genitive plural form gutani in the Pietroassa inscription. The Demonym is also attested in Greek as γόθοι, γότθοι, γόθθοι and in Latin as Gothi. The word "Goths" derives from the stem Gutan-. This stem produces the singular *Gutô, plural *Gutaniz in Proto-Germanic. It survives in the modern Scandinavian tribal name Gutes, which is what the inhabitants of the present-day Swedish island Gotland in Baltic Sea call themselves (In Gutnish - Gutar, in Swedish "Gotlänningar"). Another modern Scandinavian tribal name, Geats (in Swedish "Götar"), which is what the (original) inhabitants of present-day Götaland call themselves, derives from a related Proto-Germanic word, *Gautaz (plural *Gautôz). Both *Gautaz and *Gutô relate to the Proto-Germanic verb *geutaną, meaning "to pour". The Proto-Indo-European root of the word "geutan" and its cognates in other language is . This same root may be connected to the name of a river that flows through Västergötland in Sweden, the Göta älv, which drains Lake Vänern into the Kattegat at the city of Gothenburg. It is plausible that a flowing river would be given a name that describes it as "pouring", and that, if the original home of the Goths was near that river, they would choose an ethnonym that described them as living by the river. Another possibility is that the name of the "Geats" developed independently from that of the Gutar/Goths. The name "Goths" would eventually come to be applied to a large number of non-Gothic peoples, including Burgundians, Vandals, Gepids, Rugii, Scirii and even the non-Germanic Iranian Alans. On the basis of linguistics, these peoples, with the exception of the Alans, are often referred to as East Germanic peoples. Classification The Goths and other East Germanic-speaking groups, such as the Vandals and Gepids, eventually came to live outside of Germania, and were thereafter never considered Germani by ancient Roman authors, who consistently categorized them among the "Scythians" or other peoples who had historically inhabited the area. The Goths were Germanic-speaking. They are classified as a Germanic people by modern scholars. They are today sometimes referred to as being Germani. History Origins and early history The exact origins of the Goths are unclear and disputed. They are believed to have either originated in southern Scandinavia, in the lower Vistula area, or north of the Danube at a later date. According to Jordanes, 6th-century, the Goths migrated from southern Scandinavia to the lower Vistula, seizing the lands of the Rugii. Such a migration is controversial, and has not been confirmed archaeologically. Rather than a wholesale migration, Herwig Wolfram considers it entirely plausible that at the Gothic elite was indeed descended from southern Scandinavia. Recent genetic studies has lent support to the Scandianvian theory. The earliest possible mentions of the Goths are Roman sources of the 1st century AD, who refer to a people called the "Gutones" living along the lower Vistula. The Gutones are generally considered ancestral or even identical to the later Goths, but not everyone accepts this. The Gutones are associated with the Wielbark culture, which flourished in the area at the time, having succeeded the Oksywie culture. Roman historians write that the Gutones were in close contact with the Lugii and Vandals, and that they were at times in conflict with the Suebi. A people of Scandza called the Gutae, possibly identical to the later Geats, are also mentioned, and it's possible that this people had close relations or even shared origins with the Gutones. Evidence from etymology and the Gutasaga suggests connections with Gotland and the Gutes. During the early centuries AD, the Wielbark culture expands southward at the expense of the Przeworsk culture, which is associated with the Lugii and Vandals. By the 3rd century AD, this southward expansion to the areas north of the Danube is believed to have contributed to the formation of the Chernyakhov culture. It is in the 3rd century that the name "Goths" are first mentioned, and a minority of scholars therefore suggest that the Goths originated north of the Black Sea in the 3rd century. Jordanes and Getica The traditional account of the Goths' early history depends on the work Getica, written by the Goth Jordanes 551 AD. Getica is based on an earlier lost work by Cassiodorus, which was in turn based upon an even earlier work by the Gothic historian Ablabius. According to Jordanes the earliest migrating Goths sailed from Scandza (Scandinavia) under King Berig in three ships and named their settlement Gothiscandza, after themselves. Although the exact location of Gothiscandza is unclear, it is generally believed to have somewhere near Gdańsk. Jordanes tells us that one shipload "dwelled in the province of Spesis on an island surrounded by the shallow waters of the Vistula." From Gothiscandza, the Goths then moved into an area along the southern coast of the Baltic Sea which was inhabited by the "Ulmerugi" (Rugii), expelled them, and also subdued the neighboring Vandals. Jordanes' account is controversial, and certainly contains many inaccuracies. It has not been possible to confirm archaeologically his account of a Gothic origin in Scandinavia. Walter Goffart claims that the Getica is an entirely fabricated propaganda piece produced as part of a political conspiracy, with no foundation in oral tradition. Critics of Jordanes typically argue that since his work contains certain obvious errors, it must be entirely unreliable. Because he considers Jordanes completely unreliable, Goffart further charges that all archaeological evidence on the early Goths is unreliable, as this evidence is connected to Jordanes. Goffart's theories on Getica has by Peter Heather been rejected as a "flawed" and "unconvincing" conspiracy theory. Herwig Wolfram considers Getica to be a work of indispensable value to Gothic history. He considers it a relic of Gothic oral tradition, and believes that the Gothic elite originated in Scandinavia. Heather also suggests that Getica is partially based on authentic Gothic tradition. Jordanes' account of Gothic settlement in modern-day Poland is considered accurate by most historians. His account of an early Gothic migration from Scandinavia enjoys large support, particularly among experts in Germanic philology. Evidence from classical sources Pliny the Elder wrote that Pytheas, an explorer who visited Northern Europe in the 4th century BC, reported that the "Guiones" already inhabited the shores of an estuary of at least 6,000 stadia called Mentonomon where amber is cast up by the waves. Pliny believed this was in Germania and notes that these "Guiones" sold this amber to their neighbors, the Teutones. To fit with other evidence, some modern commentators believe these "Guiones" should be corrected to "Gutones" and that the Mentonomon is on the Baltic shore, although this is disputed by for example Christensen, who believes that the reference to a geographical "Germania" was added by Pliny. Other authors believe, for example, that the Guiones are the Ingvaeones and the Mentonomon is the North Sea coast. In an earlier chapter, describing the peoples of Germania, Pliny stated that the Gutones, along with the Burgundiones, Varini and Carini, belong to the Vandili. Pliny considers the Vandili one of the five principal "German races", along with the coastal Ingvaeones, the Rhineland Istvaeones, the Irminones and the Peucini. Strabo mentioned "Butones" together with the Lugians and Semnones and others as one of a large group of people who came under the dominance of Maroboduus of the Marcomanni, and again many modern authors argue this name should be correct to "Gutones". The Vandals and Lugians are often equated with one another. In a later work, Germania, Tacitus wrote that the Gotones/Gothones and the neighboring Rugii and Lemovii were "Germani" who carried round shields and short swords, and lived near the Ocean, beyond the Vandals. He described them as "ruled by kings, a little more strictly than the other German tribes". In his other notable work, The Annals, Tacitus writes that the Gotones had assisted Catualda, a young Macomannic exile, in overthrowing the rule of Maroboduus. The Gotones of Tacitus are usually treated as the same as the later Goths, although this has been disputed by some. Ptolemy, in the second century, mentions a people called the Gutae/Gautae, probably the same as the later Gauti mentioned by Procopius, living in southern Scandia. In a later chapter, he mentions the Gutones/Gythones east of the Vistula in Sarmatia, between the Veneti and the Fenni. Wolfram and many other scholars on the Goths considers it likely that there were close connections between then Gutones and Gutae, and that they were possibly two branches of the same people. Ancient authors do not equate the Gutones with the Goths. The equation is nevertheless supported by Herwig Wolfram, Peter Heather, and among scholars in general. Philologists and linguists have no doubts and consider it indisputable that these are the same names. Historian Arne Søby Christensen has argued that the Gutones and similarly named peoples mentioned by early Roman authors were possibly not identical to the Goths, but concedes that such an equation is generally accepted and is chronologically a "realistic possibility". Christensen's theories have rejected as "based on dubious reasoning" and "surely too extreme" by other historians such as Michael Whitby, who considers them "little more than a long footnote" to what has already been published on the subject by Peter Heather and others. Other literary evidence The 5th century Hispano-Roman historian Orosius wrote that the Goths were of the same stock as the Suiones (Swedes), the Vandals, and the other Scandinavian (North Germanic) tribes. Procopius noted that the Goths, Gepids and Vandals were physically and culturally identical, suggesting a common origin. According to Isidore of Seville, the Goths were descended from Gog and Magog, and of the same race as the Getae. Archaeological evidence The early Goths are associated with the Wielbark culture. The Swedish archaeologist Anders Kaliff believes that this culture largely developed from earlier cultures in Pomerania. According to the Polish archaeologist Andrzej Kokowski however, it replaced the local Oksywie culture in the 1st century AD, when a Scandinavian settlement developed in a buffer zone between the Oksywie culture and the Przeworsk culture. Sometime around the 1st century AD, there may have been a large migration out of Scandinavia. Early archaeological evidence in the traditional Swedish province of Östergötland suggests a general depopulation during this period. However, there is no archaeological evidence for a substantial emigration from Scandinavia, A Scandinavian origin of the Goths can therefore not be confirmed archaeologically. Frederik Kortlandt has suggested that they originated in continental Europe. Archaeological finds show close contacts between southern Sweden and the Baltic coastal area on the continent, and further towards the south-east, evidenced by pottery, house types and graves. Rather than a massive migration, similarities in the material cultures may be products of long-term regular contacts. However, the archaeological record could indicate that while his work is thought to be unreliable, Jordanes' story was based on an oral tradition with some basis in fact. The settlement in today's Poland may correspond to the introduction of Scandinavian burial traditions, such as the stone circles and the stelae especially common on the island of Gotland and other parts of southern Sweden. The Chernyakhov culture, which emerged on the Pontic steppe in the 3rd century AD, displays close similarities with the Wielbark culture, and it thought to have been largely derived through a southward expansion of Wielbark. The Chernyakhov culture is universally believed to have been dominated by the Goths and related Germanic peoples. Certain scholars, such as Walter Goffart, completely ignore archaeological evidence on the Goths. They contend that archaeological evidence on the Goths is largely derived from Jordanes, and because they consider Jordanes unreliable, this makes archaeological evidence on the Goths unreliable as well. Genetic evidence A 2019 genetic study published in Scientific Reports examined the remains of individuals identified with the Wielbark culture and the Goths. Close genetic relations to populations of Iron Age Scandinavia and modern Norwegians and Swedes were detected, The authors of the study cited this as supporting the theory of a Scandinavian origin of the Goths. In 2019, a genetic study of various cultures of the Eurasian Steppe was published in Current Biology. Samples from three individuals thought to belong to the Gothic component of the Chernyakhov culture were analyzed. The results appeared to confirm the theory that the Chernyakhov culture emerged as a result of a Gothic migration from the north. Evidence from historical parallels The Goths were neither the first nor the only Germanic people who migrated south-eastward towards the Black Sea from a probable northern homeland. Several centuries earlier, the Bastarnae had made a similar migration, only to be overwhelmed by the Sarmatians in the 1st century AD. Contemporary with the suggested Gothic migration, there was also confirmed migrations of Rugii, Vandals, Burgundians and other Germanic tribes towards the south-east. These historical parallels gives credit to the theory that the Goths also emerged on the Danube through a migration from further north. Linguistic evidence Gothic is part of the East Germanic branch of the Germanic languages, and through the Gothic Bible of the 4th century AD it is the oldest Germanic language attested. The fact that the Goths were Germanic-speaking and carried Germanic names suggests an origin far to the northwest of the Black Sea. The fact that their language was maintained through centuries of migration suggests these migrations involved not only elite males, but also women and children. Evidence from the sagas In medieval Scandinavia, the area of the lower Vistula were remembered as Gothic lands. Both the Goths and the Gutes were called Gotar in Old West Norse, and Gutar in Old East Norse (for example in the Gutasaga and in runic inscription on the Rökstone). In contrast, the other tribe, the Geats, were clearly differentiated from the Goths / Gutes. Since Old Norse literature does not distinguish between the Goths and the Gutes, but does clearly distinguish between the Goths or Gutes on the one hand, and the Geats on the other (as does Old English literature), it is plausible that the Goths supposed to have migrated out of Scandinavia were members of the Gutes tribe. The Gotlanders themselves have oral traditions of a mass migration towards southern Europe, recorded in the Gutasaga. If the facts are related, this would be a unique case of a tradition that endured for more than a thousand years and that actually pre-dates most of the major splits in the Germanic language family. Migration to the Black Sea and the formation of the Chernyakhov culture Beginning in the middle 2nd century, the Gothic Wielbark culture shifted to the southeast, towards the Black Sea. The part of the Wielbark culture that moved was the oldest portion, located west of the Vistula and still practicing Scandinavian burial traditions. It has been suggested that the Goths maintained contact with southern Sweden during their migration. Around 160 AD, in Central Europe, the first movements of the Migration Period were occurring, as several Germanic tribes, such as the Rugii, Goths, Gepids, Vandals and Burgundians, began moving south-east from their ancestral lands, putting pressure on their southern neighboors. As a result, other Germanic tribes were pushed towards the Roman Empire, leading to the Marcomannic Wars. This conflict resulted in widespread destruction and the first invasion of what is now Italy in the Roman Empire period. The source of the turmoil occurring in Germania at the time has been ascribed to population growth. During this time the Gothic Wielbark culture is believed to have ejected and partially absorbed the people of the Przeworsk culture, who are connected to the Vandals. By 200 AD, Wielbark Goths were probably being recruited into the Roman army. According to Jordanes, the Goths entered Oium, part of Scythia, under their king Filimer, where they subdued the Spali (Sarmatians). On the Pontic Steppe, the Goths installed themselves as the rulers of the local Zarubintsy culture, forming the new Chernyakhov culture (c. 250 – c. 400). This strikingly uniform culture came to be stretch from the Danube in the west to the Don in the east. The Chernyakhov culture is believed to have been dominated by the Goths and other Germanic groups such as the Heruli. It nevertheless also included Iranian, Dacian, Roman and probably Slavic elements as well. The Germanic Bastarnae had made a similar migration as the Goths centuries earlier, only to be defeated by Sarmatians in the 1st century. The replacement of the Sarmatians by a new Germanic elite thus constituted another major cultural shift in the area. The first Greek references to the Goths call them Scythians, since this area, known as Scythia, had historically had been occupied by an unrelated people of that name. The application of that designation to the Goths appears to be not ethnological but rather geographical and cultural - Greeks regarded both the ethnic Scythians and the Goths as "barbarians". A minority of scholars insist that the Goths did not exist until being mentioned by the Romans in the 3rd century AD. Upon their arrival on the Pontic Steppe, the Goths quickly adopted several nomadic customs from the Sarmatians. They came to excel at horsemanship, archery and falconry, and were also accomplished agriculturalists and seafarers. J. B. Bury describes the Gothic period as "the only non-nomadic episode in the history of the steppe." William H. McNeill compares the migration of the Goths to that of the early Mongols, who migrated southward from the forests and came to dominate the eastern Eurasian steppe around the same time as the Goths in the west. Early raids on the Roman Empire In the first attested incursion in Thrace, the Goths were mentioned as Boranoi by Zosimus, and then as Boradoi by Gregory Thaumaturgus. The first incursion of the Roman Empire that can be attributed to Goths is the sack of Histria in 238. Several such raids followed in subsequent decades, in particular the Battle of Abrittus in 251, led by Cniva, in which the Roman Emperor Decius was killed. This was one of the most disastrious defeats in the history of the Roman army. By this time, there were at least two groups of Goths, who were separated by the Dniester River: the Thervingi and the Greuthungi. Goths were at the time heavily recruited into the Roman Army to fight in the Roman-Persian Wars, notably participating at the Battle of Misiche in 242. The first seaborne raids took place in three subsequent years, probably 255-257. An unsuccessful attack on Pityus was followed in the second year by another, which sacked Pityus and Trabzon and ravaged large areas in the Pontus. In the third year, a much larger force devastated large areas of Bithynia and the Propontis, including the cities of Chalcedon, Nicomedia, Nicaea, Apamea Myrlea, Cius and Bursa. By the end of the raids, the Goths had seized control over Crimea and the Bosporus and captured several cities on the Euxine coast, including Olbia and Tyras, which enabled them to engage in widespread naval activities. After a 10-year gap, the Goths, along with the Heruli, raiding on 500 ships, sacked Heraclea Pontica, Cyzicus and Byzantium. They were defeated by the Roman navy but managed to escape into the Aegean Sea, where they ravaged the islands of Lemnos and Scyros, broke through Thermopylae and sacked several cities of southern Greece (province of Achaea) including Athens, Corinth, Argos, Olympia and Sparta. Then an Athenian militia, led by the historian Dexippus, pushed the invaders to the north where they were intercepted by the Roman army under Gallienus. He won an important victory near the Nessos (Nestos) river, on the boundary between Macedonia and Thrace, the Dalmatian cavalry of the Roman army earning a reputation as good fighters. Reported barbarian casualties were 3,000 men. Subsequently, the Heruli leader Naulobatus came to terms with the Romans. After Gallienus was assassinated outside Milan in the summer of 268 in a plot led by high officers in his army, Claudius was proclaimed emperor and headed to Rome to establish his rule. Claudius' immediate concerns were with the Alamanni, who had invaded Raetia and Italy. After he defeated them in the Battle of Lake Benacus, he was finally able to take care of the invasions in the Balkan provinces. In the meantime, a second and larger sea-borne invasion had started. An enormous coalition consisting of Goths (Greuthungi and Thervingi), Gepids and Peucini, led again by the Heruli, assembled at the mouth of river Tyras (Dniester). The Augustan History and Zosimus claim a total number of 2,000–6,000 ships and 325,000 men. This is probably a gross exaggeration but remains indicative of the scale of the invasion. After failing to storm some towns on the coasts of the western Black Sea and the Danube (Tomi, Marcianopolis), the invaders attacked Byzantium and Chrysopolis. Part of their fleet was wrecked, either because of the Gothic inexperience in sailing through the violent currents of the Propontis or because it was defeated by the Roman navy. Then they entered the Aegean Sea and a detachment ravaged the Aegean islands as far as Crete, Rhodes and Cyprus. The fleet probably also sacked Troy and Ephesus, destroying the Temple of Artemis, one of the Seven Wonders of the Ancient World. While their main force had constructed siege works and was close to taking the cities of Thessalonica and Cassandreia, it retreated to the Balkan interior at the news that the emperor was advancing. Learning of the approach of Claudius, the Goths first attempt to directly invade Italy. They are engaged near Naissus by a Roman army led by Claudius advancing from the north. The battle most likely took place in 269, and was fiercely contested. Large numbers on both sides were killed but, at the critical point, the Romans tricked the Goths into an ambush by pretended flight. Some 50,000 Goths were allegedly killed or taken captive and their base at Thessalonika destroyed. It seems that Aurelian who was in charge of all Roman cavalry during Claudius' reign, led the decisive attack in the battle. Some survivors were resettled within the empire, while others were incorporated into the Roman army. The battle ensured the survival of the Roman Empire for another two centuries. In 270, after the death of Claudius, Goths under the leadership of Cannabaudes again launched an invasion on the Roman Empire, but were defeated by Aurelian, who however surrendered Dacia beyond the Danube. Around 275 the Goths launched a last major assault on Asia Minor, where piracy by Black Sea Goths was causing great trouble in Colchis, Pontus, Cappadocia, Galatia and even Cilicia. They were defeated sometime in 276 by Emperor Marcus Claudius Tacitus. In the late 3rd century, as recorded by Jordanes, the Gepids, under their king Fastida, utterly defeated the Burgundians, and then attacked the Goths and their king Ostrogotha. Out of this conflict, Ostrogotha and the Goths emerged victorious. In the last decades of the 3rd century AD, large number of Capri are recored as fleeing Dacia for the Roman Empire, having probably been evicted from the area by Goths. Co-existence with the Roman Empire In 332, Constantine helped the Sarmatians to settle on the north banks of the Danube to defend against the Goths' attacks and thereby enforce the Roman border. Around 100,000 Goths were reportedly killed in battle, and Aoric, son of the Thervingian king Ariaric, was captured. Eusebius, an historian who wrote in Greek in the third century, wrote that in 334, Constantine evacuated approximately 300,000 Sarmatians from the north bank of the Danube after a revolt of the Sarmatians' slaves. From 335 to 336, Constantine, continuing his Danube campaign, defeated many Gothic tribes. Having been driven from the Danube by the Romans, the Thervingi invaded the territoy of the Sarmatians of the Tisza. In this conflict, the Thervingi were led by Vidigoia, "the bravest of the Goths" and were victorious, although Vidigoia was killed. Jordanes states that Aoric was succeeded by Geberic, "a man renowned for his valor and noble birth", who waged war on the Hasdingi Vandals and their king Visimar, forcing them to settle in Pannonia under Roman protection. Both the Greuthungi and Thervingi became heavily Romanized during the 4th Century. This came about through trade with the Romans, as well as through Gothic membership of a military covenant, which was based in Byzantium and involved pledges of military assistance. Reportedly, 40,000 Goths were brought by Constantine to defend Constantinople in his later reign, and the Palace Guard was thereafter mostly composed of Germanic warriors, as Roman soldiers by this time had largely lost military value. The Goths increasingly became soldiers in the Roman armies in the 4th Century AD leading to a significant Germanization of the Roman Army. Without the recruitment of Germanic warriors in the Roman Army, the Roman Empire would not have survived for as long as it did. Goths who gained prominent positions in the Roman military include Gainas, Tribigild, Fravitta and Aspar. Mardonius, a Gothic eunuch, was the childhood tutor and later adviser of Roman emperor Julian, on whom he had an immense influence. The Gothic penchant for wearing skins became fashion in Constantinople, which was heavily denounced by conservatives. The 4th century Greek historian Eunapius described the Goths' powerful build in a pejorative way: "Their bodies provoked contempt in all who saw them, for they were far too big and far too heavy for their feet to carry them, and they were pinched in at the waist – just like those insects Aristotle writes of." The 4th century Greek bishop Synesius compared the Goths to wolves among sheep, mocked them for wearing skins and questioned their loyalty towards Rome: A man in skins leading warriors who wear the chlamys, exchanging his sheepskins for the toga to debate with Roman magistrates and perhaps even sit next to a Roman consul, while law-abiding men sit behind. Then these same men, once they have gone a little way from the senate house, put on their sheepskins again, and when they have rejoined their fellows they mock the toga, saying that they cannot comfortably draw their swords in it. In the 4th century, the Gothic missionary Wulfila devised the Gothic alphabet to translate the Wulfila Bible and converted many of the Goths from Germanic paganism to Arian Christianity. In the 4th century, Geberic was succeeded by the Greuthungian king Ermanaric, who embarked on a large-scale expansion. Jordanes states that Ermanaric conquered a large number of warlike tribes, including the Heruli (who were led by Alaric), the Aesti and the Vistula Veneti, who, although militarily weak, were very numerous, and took up a strong fight. Jordanes compares the conquests of Ermanaric to those of Alexander the Great, and states that he "ruled all the nations of Scythia and Germany by his own prowess alone." Interpreting Jordanes, Herwig Wolfram estimates that Ermanaric dominated a vast area of the Pontic Steppe stretching from the Baltic Sea to the Black Sea as far eastwards as the Ural Mountains, encompassing not only Greuthungi, but also Finnic peoples, Slavs (such as the Antes), Rosomoni (Roxolani), Alans, Huns, Sarmatians and probably Aestii (Balts). According to Wolfram, it is certainly possible that the sphere of influence of the Chernyakhov culture could have extended well beyond its archaeological extent. Chernyakhov finds have indeed been found far to the north in the forest steppe, suggesting Gothic domination of this area. Peter Heather on the other hand, contends that the extent of Ermanaric's power is exaggerated. Ermanaric's possible dominance of the Volga-Don trade routes has made historian Gottfried Schramm consider his realm as a forerunner of the Viking founded state of Kievan Rus'. In the western part of Gothic territories, dominated by the Thervingi, there were also populations of Taifali, Sarmatians and other Iranian peoples, Dacians, Daco-Romans and other Romanized populations. According to Hervarar saga ok Heiðreks (The Saga of Hervör and Heidrek), a 13th-century legendary saga, Árheimar was the capital of Reidgotaland, the land of the Goths. The saga states that it was located on the Dnieper river. Jordanes refers to the region as Oium. In the 360s, Athanaric, son of Aoric and leader of the Thervingi, supported the usurper Procopius against the Eastern Roman Emperor Valens. In retaliation, Valens invaded the territories of Athanaric and defeated him, but was unable to achieve a decisive victory. Athanaric and Valens thereupon negotiated a peace treaty, favorable to the Thervingi, on a boat at the Danube river, as Athanaric refused to set his feet within the Roman Empire. Soon afterwards, Fritigern, a rival of Athanaric, converted to Arianism, gaining the favor of Valens. Athanaric and Fritigern thereafter fought a civil war in which Athanaric appears to have been victorious. Athanaric thereafter carried out a crackdown on Christianity in his realm. Arrival of the Huns Around 375 AD the Huns overran the Alans, an Iranian people living to the east of the Goths, and then, along with Alans, invaded the Goths themselves. A source for this period is Ammianus Marcellinus. He wrote that Hunnic domination of the Gothic kingdoms in Scythia began in the 370s. It is possible that the Hunnic attack came as a response to the Gothic eastwards expansion. Upon the suicide of Ermanaric, the Greuthungi gradually fell under Hunnic dominance. Christopher I. Beckwith suggests that the Hunnic thrust into Europe and the Roman Empire was an attempt to subdue independent Goths in the west. The Huns fell upon the Thervingi, and Athanaric sought refuge in the mountains (referred to as Caucaland in the sagas). Ambrose makes a passing reference to Athanaric's royal titles before 376 in his De Spiritu Sancto (On the Holy Ghost) Battles between the Goths and the Huns are described in the Hlöðskviða (The Battle of the Goths and Huns), a medieval Icelandic saga. The sagas recall that Gizur, king of the Geats, came to the aid of the Goths in an epic conflict with the Huns, although this saga might derive from a later Gothic-Hunnic conflict. Although the Huns successfully subdued many of the Goths, who joined their ranks, Fritigern approached the Eastern Roman emperor Valens in 376 with a portion of his people and asked to be allowed to settle on the south bank of the Danube. Valens permitted this, and even assisted the Goths in their crossing of the river (probably at the fortress of Durostorum). The Gothic evacuation across the Danube was probably not spontaneous, but rather a carefully planned operation initated after long debate among leading members of the community. Upon arrival, the Goths were to be disarmed as according to their agreement with the Romans, although many of them still managed to keep their arms. The Moesogoths settled in Thrace and Moesia. The Gothic War Mistreated by corrupt local Roman officials, the Gothic refugees were soon experiencing a famine; some are recorded having being forced to sell their children to Roman slave traders in return for rotten dog meat. Enraged by this treachery, Fritigern unleashed a widescale rebellion in Thrace, in which he was joined not only by Gothic refugees and slaves, but also by disgruntled Roman workers and peasants, and Gothic deserters from the Roman Army. The ensuing conflict, known as the Gothic War, lasted for several years. Meanwhile, a group of Greuthungi, led by the chieftains Alatheus and Saphrax, who were co-regents for Vithericus, son and heir of the Greuthungi king Vithimiris, crossed the Danube without Roman permission. The Gothic War culminated in the Battle of Adrianople in 378, in which the Romans were badly defeated and Valens was killed. Following the decisive Gothic victory at Adrianople, Julius, the magister militum of the Eastern Roman Empire, organized a wholesale massacre of Goths in Asia Minor, Syria and other parts of the Roman East. Fearing rebellion, Julian lured the Goths into the confines of urban streets from which they could not escape and massacred soldiers and civilians alike. As word spread, the Goths rioted throughout the region, and large numbers were killed. Survivors may have settled in Phrygia. With the rise of Theodosius I in 379, the Romans launched a renewed offensive to subdue Fritigern and his followers. Around the same time, Athanaric arrived in Constantinople, having fled Caucaland through the scheming of Fritigern. Athanaric received a warm reception by Theodosius, praising the Roman Emperor in return, and was awarded a magnificent funeral by the emperor following his death shortly after his arrival. In 382, Theodosius decided to enter peace negotiations with the Thervingi, which were concluded on 3 October 382. The Thervingi were subsequently made foederati of the Romans in Thrace and obliged to provide troops to the Roman army. Later division and spread of the Goths In the aftermath of the Hunnic onslaught, two major groups of the Goths would eventually emerge, the Visigoths and Ostrogoths. The Visigoths, led by the Balti dynasty, claimed descend from the Thervingi and lived as foederati inside Roman territory, while the Ostrogoths, led by the Amali dynasty, claimed descent from the Greuthungi and were subjects of the Huns. Procopius interpreted the name Visigoth as "western Goths" and the name Ostrogoth as "eastern Goth", reflecting the geographic distribution of the Gothic realms at that time. A people closely related to the Goths, the Gepids, were also living under Hunnic domination. A smaller group of Goths were the Crimean Goths, who remained in Crimea and maintained their Gothic identity well into the Middle Ages. Visigoths Following Theodosius' treaty, Visigoths received prominent positions in the Roman army. Relations with Roman civilians were sometimes uneasy; in 391, Gothic soldiers, with the blessing of Theodosius I, massacred thousands of Roman spectators at the Hippodrome in Thessalonica as vengeance for the lynching of the Gothic general Butheric. The Visigoths suffered heavy losses while serving Theodosius in the civil war of 394 against Eugenius and Arbogast. In 395, following the death of Theodosius I, the Visigoths elected Alaric I as their king and invaded Greece, where they sacked Piraeus (the port of Athens) and destroyed Corinth, Megara, Argos, and Sparta. Athens was spared by paying a large bribe, and the Eastern emperor Flavius Arcadius subsequently appointed Alaric magister militum (“master of the soldiers”) in Illyricum in 397. In 401 and 402, Alaric made two attempts at invading Italy, but was defeated by Stilicho. In 405-406, another Gothic leader, Radagaisus, also attempted to invade Italy, and was also defeated by Stilicho. In 408, the Western Roman emperor Flavius Honorius ordered the execution of Stilicho and his family, then incited the Roman population to massacre tens of thousands of wives and children of Goths serving in the Roman military. Subsequently, around 30,000 Gothic soldiers defected to Alaric. Alaric in turn invaded Italy, seeking to pressure Honorious into granting him permission to settle his people in North Africa. In Italy, Alaric liberated tens of thousands of Gothic slaves, and in 410 he sacked the city of Rome. Although the city's riches were plundered, the civilian inhabitants of the city were treated humanely, and only a few buildings were burned. Alaric died soon afterwards, and was buried along with his treasure in an unknown grave under the Busento river. Alaric was succeeded by his brother-in-law Athaulf, who was married to Honorius' sister Galla Placidia, who had been seized during Alaric's sack of Rome. Athaulf settled the Visigoths in southern Gaul. After failing to gain recognition from the Romans, Athaulf retreated into Hispania in early 415, and was assassinated in Barcelona shortly afterwards. He was succeeded by Sigeric and then Wallia, who succeeded in having the Visigoths accepted by Honorius as foederati in southern Gaul with their capital at Toulouse. Wallia subsequently inflicted severe defeats upon the Silingi Vandals and the Alans in Hispania. Periodically they marched on Arles, the seat of the praetorian prefect but were always pushed back. In 437 the Visigoths signed a treaty with the Romans which they kept. Under Theodoric I the Visigoths allied with the Romans and fought Attila to a stalemate in the Battle of the Catalaunian Fields, although Theodoric was killed in the battle. Under Euric, the Visigoths established an independent Visigothic Kingdom and succeeded in driving the Suebi out of Hispania proper and back into Galicia. Although the barbarians controlled Spain, they still formed a tiny minority among a much larger Hispano-Roman population, approximately 200,000 out of 6,000,000. In 507, the Visigoths were pushed out of most of Gaul by the Frankish king Clovis I at the Battle of Vouillé. They were able to retain Narbonensis and Provence after the timely arrival of an Ostrogoth detachment sent by Theodoric the Great. The defeat at Vouillé resulted in their further penetration of Hispania and establishment of a new capital at Toledo. Under Liuvigild in the latter part of the 6th century, they succeeded in subduing the Suebi in Gallicia and the Byzantines in the south-west, achieving dominance over most of the peninsula. Liuvigild also abolished the law which prevented intermarriage between Hispano-Romans and Goths, and he remained an Arian Christian. The conversion of Reccared I to Roman Catholicism in the late 6th century prompted the assimilation of Goths and Hispano-Romans. At the end of the 7th century, the Visigothic Kingdom began to suffer from internal troubles. Their kingdom fell and progressively to conquered by the Umayyad Caliphate from 711 after the defeat of their last king Roderic at the Battle of Guadalete. Some nobles found refuge in the mountain areas of the Pyrenees and Cantabria. The Christians began to regain control under the leadership of the Visigothic nobleman Pelagius of Asturias, who founded the Kingdom of Asturias in 718 and defeated the Muslims at the Battle of Covadonga in ca. 722, in what is taken to be the beginning of the Reconquista. It was from the Asturian kingdom that modern Spain and Portugal evolved. The Visigoths never became completely Romanized, as they became rather 'Hispanicized' and further became widespread over a large territory and body of population. They progressively adopted a new culture, retaining little of their original culture except for practical military customs, some artistic modalities, family traditions such as heroic songs and folklore, as well as select conventions to include Germanic names still in use in present-day Spain. It is these artifacts of the original Visigothic culture that give ample evidence of its contributing foundation for the present regional culture. Portraying themselves heirs of the Visigoths, the subsequent Christian Spanish monarchs declared their responsibility for the Reconquista of Islamic Spain, which was completed with the Fall of Granada in 1492. Ostrogoths After the Hunnic invasion, many Goths became subjects of the Huns. These would become known as the Ostrogoths. Others sought refuge in the Roman Empire, where many of them were recruited into the Roman army. In the spring of 399, Tribigild, a Gothic leader in charge of troops in Nakoleia, rose up in rebellion and defeated the first imperial army sent against him, possibly seeking to emulate Alaric's successes in the west. Gainas, a Goth who along with Stilicho and Eutropius had deposed Rufinus in 395, was sent to suppress Tribigild's rebellion, but instead plotted to use the situation to seize power in the Eastern Roman Empire. This attempt was however thwarted by the pro-Roman Goth Fravitta, and in the aftermath, thousands of Gothic civilians were massacred in Constantinople, many being burned alive in the local Arian church where they had taken shelter. As late as the 6th century Goths were settled as foederati in parts of Asia Minor. Their descendants, who formed the elite Optimatoi regiment, still lived there in the early 8th century. While they were largely assimilated, their Gothic origin was still well-known: the chronicler Theophanes the Confessor calls them Gothograeci. The Ostrogoths fought together with the Huns at the Battle of the Catalaunian Plains in 451. Following the death of Attila and the defeat of the Huns at the Battle of Nedao in 454, the Ostrogoths broke away from Hunnic rule under their king Valamir. Under his successor, Theodemir, they utterly defeated the Huns at the Bassianae in 468, and then defeated a coalition of Roman-supported Germanic tribes at the Battle of Bolia in 469, which gained them supremacy in Pannonia. Theodemir was succeeded by his son Theodoric in 471, who was forced to compete with Theodoric Strabo, leader of the Thracian Goths, for the leadership of his people. Afraid of the threat posed by Theodoric to Constantinople, the Eastern Roman emperor Zeno ordered Theodoric to invade Italy in 488. By 493, Theodoric had conquered all of Italy from the Scirian Odoacer, whom he killed with his own hands. Theodoric subsequently formed the Ostrogothic Kingdom. Theodoric settled his entire people in Italy, estimated at 100,000-200,000, mostly in the northern part of the country, and ruled the country very efficiently. The Goths in Italy constituted a small minority of the population in the country. Intermarriage between Goths and Romans were forbidden, and Romans were also forbidden from carrying arms. Nevertheless, the Roman majority was treated fairly. The Goths were briefly reunited under one crown in the early 6th century under Theodoric, who became regent of the Visigothic kingdom following the death of Alaric II at the Battle of Vouillé in 507. Shortly after Theodoric's death, the country was invaded by the Eastern Roman Empire in the Gothic War, which severely devastated and depopulated the Italian peninsula. The Ostrogoths made a brief resurgence under their efficient king Totila, who was however killed at the Battle of Taginae in 552. After the last stand of the Ostrogothic king Teia at the Battle of Mons Lactarius in 553, Ostrogothic resistance ended, and the remaining Goths in Italy were assimilated by the Lombards, another Germanic tribe, who invaded Italy and founded the Kingdom of the Lombards in 567 AD. Crimean Goths Gothic tribes who remained in the lands around the Black Sea, especially in Crimea - were known as the Crimean Goths. During the late 5th and early 6th century, the Crimean Goths had to fight off hordes of Huns who were migrating back eastward after losing control of their European empire. In the 5th century, Theodoric the Great tried to recruit Crimean Goths for his campaigns in Italy, but few showed interest in joining him. They became affiliated with the Eastern Orthodox Church through the Metropolitanate of Gothia, and became closely associated with the Byzantine Empire. In the Middle Ages, the Crimean Goths were in perpetual conflict with the Khazars. John of Gothia, the metropolitan bishop of Doros, capital of the Crimean Goths, briefly expelled the Khazars from Crimea in the late 8th century, and was subsequently canonized as an Eastern Orthodox saint. In the 10th century, the lands of Crimean Goths were once again raided by the Khazars. As a response, the leaders of the Crimean Goths made an alliance with Sviatoslav I of Kiev, who subsequently waged war upon and utterly destroyed the Khazar Khaganate. In the late Middle Ages the Crimean Goths were part of the Principality of Theodoro, which was conquered by the Ottoman Empire in the late 15th century. As late as the 18th century a small number of people in Crimea may still have spoken Crimean Gothic. Physical appearance In ancient sources, the Goths are always described as tall and athletic, with light skin, blonde hair and blue eyes. Their physical size became a source of contempt among the Romans. Procopius notes that the Vandals and Gepids looked similar to the Goths, and on this basis, he suggested that they were all of common origin. Of the Goths, he wrote that "they all have white bodies and fair hair, and are tall and handsome to look upon." Genetics A genetic study published in Scientific Reports in 2018 examined the mtDNA of 60 individuals buried at the Wielbark cemetery of Kowalewko in the 1st and 2nd centuries AD. The majority of the individuals carried types of haplogroup H and U, and notably displayed higher frequencies of U5b (a typically Western Hunter-Gatherer lineage) than preceding and succeeding populations in the area. They were found to be most closely related to Iron Age Scandinavian populations and the Bell Beaker culture. Strong genetic similarities with modern Scandinavians, such as Norwegians and Swedes, were detected. The males and females of Kowalewko were found to be of significantly different origins, with males displaying closer links to Iron Age Scandinavia and carrying higher amounts of steppe ancestry and hunter-gatherer ancestry than the females. A genetic study published in Scientific Reports in 2019 examined the mtDNA of 27 Goths buried at a Wielbark cemetery in Masłomęcz from the 2nd to the 4th centuries AD. They were found to be mostly carriers of haplogroup H and U. The individuals displayed even closer genetic links to Iron Age Scandinavian populations than those of Kowalewko did. Males and females at Masłomęcz were found to be more closely related to each other than those at Kowalewko were. They also carried fewer samples of U5b, and displayed less strong genetic links to the steppe than earlier Wielbark samples from Kowalewko. The results appeared to support the theory that the Goths originated in southern Scandinavia and expanded southwards through the Wielbark culture towards the Black Sea, where they mixed with local populations and established the Chernyakhov culture. A genetic study published in Scientific Reports in 2019 examined the mtDNA of three Gothic females from the Chernyakhov culture. They carried haplogroup H1n6, H1c and T2g1 respectively. These individuals were genetically significantly different from previous populations of the area, being distinguished by a higher amount of ancestry from western and northern Europe. The results appeared to confirm the theory that the Chernyakhov culture emerged as a result of a Gothic migration from the north. Culture Art Before the invasion of the Huns, the Gothic Chernyakhov culture produced jewelry, vessels, and decorative objects in a style much influenced by Greek and Roman craftsmen. They developed a polychrome style of gold work, using wrought cells or setting to encrust gemstones into their gold objects. Language The Gothic language is the Germanic language with the earliest attestation (300s), making it a language of interest in comparative linguistics. All other East Germanic languages are known, if at all, from proper names or short phrases that survived in historical accounts, and from loan-words in other languages. It is known primarily from the Codex Argenteus, a translation of the Bible. The language was in decline by the mid-500s, due to the military victory of the Franks, the elimination of the Goths in Italy, and geographic isolation. In Spain the language lost its last and probably already declining function as a church language when the Visigoths converted to Catholicism in 589. The language survived as a domestic language in the Iberian peninsula (modern Spain and Portugal) as late as the 8th century, and Frankish author Walafrid Strabo wrote that it was still spoken in the lower Danube area in the early 9th century. In pockets of Crimea, a related dialect known as Crimean Gothic survived up until the early modern period, and the 4th-century Bible translation was in use there until at least the ninth century. Society Archaeological evidence in Visigothic cemeteries shows that social stratification was analogous to that of the village of Sabbas the Goth. The majority of villagers were common peasants. Paupers were buried with funeral rites, unlike slaves. In a village of 50 to 100 people, there were four or five elite couples. In Eastern Europe, houses include sunken-floored dwellings, surface dwellings, and stall-houses. The largest known settlement is the Criuleni District. Chernyakhov cemeteries feature both cremation and inhumation burials; among the latter the head is to the north. Some graves were left empty. Grave goods often include pottery, bone combs, and iron tools, but hardly ever weapons. Peter Heather suggest that the freemen constituted the core of Gothic society. These were ranked below the nobility, but above the freedmen and slaves. It is estimated that around a quarter to a fifth of weapon-bearing Gothic males of the Ostrogothic Kingdom were freemen. Law Warfare Economy Archaeology shows that the Visigoths, unlike the Ostrogoths, were predominantly farmers. They sowed wheat, barley, rye, and flax. They also raised pigs, poultry, and goats. Horses and donkeys were raised as working animals and fed with hay. Sheep were raised for their wool, which they fashioned into clothing. Archaeology indicates they were skilled potters and blacksmiths. When peace treaties were negotiated with the Romans, the Goths demanded free trade. Imports from Rome included wine and cooking-oil. Roman writers note that the Goths neither claimed taxes from their own nor their subjects. The early 5th century Christian writer Salvian compared the Goths' and related people's favourable treatment of the poor to the miserable state of peasants in Roman Gaul: For in the Gothic country the barbarians are so far from tolerating this sort of oppression that not even Romans who live among them have to bear it. Hence all the Romans in that region have but one desire, that they may never have to return to the Roman jurisdiction. It is the unanimous prayer of the Roman people in that district that they may be permitted to continue to lead their present life among the barbarians. Religion Initially practising Gothic paganism, the Goths were gradually converted to Arianism in the course of the 4th Century as a result of the missionary activity by the Gothic bishop Ulfilas, who devised a Gothic alphabet to write the Gothic Bible. During the 370s, Goths converting to Christianity were subject to persecution by the Thervingian king Athanaric, who was a pagan. The Visigothic Kingdom in Hispania converted to Roman Catholicism in the late 6th Century. The Ostrogoths (and their remnants, the Crimean Goths) were closely connected to the Patriarchate of Constantinople from the 5th Century, and became fully incorporated under the Metropolitanate of Gothia from the 9th Century. Legacy The Goths' relationship with Sweden became an important part of Swedish nationalism, and until the 19th Century, before the Gothic origin had been thoroughly researched by archaeologists, Swedish scholars considered Swedes to be the direct descendants of the Goths. Today, scholars identify this as a cultural movement called Gothicismus, which included an enthusiasm for things Old Norse. In Medieval and Modern Spain, the Visigoths were believed to be the origin of the Spanish nobility (compare Gobineau for a similar French idea). By the early 7th Century, the ethnic distinction between Visigoths and Hispano-Romans had all but disappeared, but recognition of a Gothic origin, e.g. on gravestones, still survived among the nobility. The 7th century Visigothic aristocracy saw itself as bearers of a particular Gothic consciousness and as guardians of old traditions such as Germanic namegiving; probably these traditions were on the whole restricted to the family sphere (Hispano-Roman nobles did service for Visigothic nobles already in the 5th century and the two branches of Spanish aristocracy had fully adopted similar customs two centuries later). Beginning in 1278, when Magnus III of Sweden ascended to the throne, a reference to Gothic origins was included in the title of the King of Sweden: In 1973, with the death of King Gustaf VI Adolf, the title was changed to simply "King of Sweden." The Spanish and Swedish claims of Gothic origins led to a clash at the Council of Basel in 1434. Before the assembled cardinals and delegations could engage in theological discussion, they had to decide how to sit during the proceedings. The delegations from the more prominent nations argued that they should sit closest to the Pope, and there were also disputes over who were to have the finest chairs and who were to have their chairs on mats. In some cases, they compromised so that some would have half a chair leg on the rim of a mat. In this conflict, Nicolaus Ragvaldi, bishop of the Diocese of Växjö, claimed that the Swedes were the descendants of the great Goths, and that the people of Västergötland (Westrogothia in Latin) were the Visigoths and the people of Östergötland (Ostrogothia in Latin) were the Ostrogoths. The Spanish delegation retorted that it was only the "lazy" and "unenterprising" Goths who had remained in Sweden, whereas the "heroic" Goths had left Sweden, invaded the Roman empire and settled in Spain. In Spain, a man acting with arrogance would be said to be "haciéndose los godos" ("making himself to act like the Goths"). In Chile, Argentina and the Canary Islands, godo was an ethnic slur used against European Spaniards, who in the early colony period often felt superior to the people born locally (criollos). A large amount of literature has been produced on the Goths, with Henry Bradley's The Goths (1888) being the standard English-language text for many decades. More recently, Peter Heather has established himself that the leading authority on the Goths in the English-speaking world. The leading authority on the Goths in the German-speaking world is Herwig Wolfram. List of early literature on the Goths In the sagas Gutasaga Hervarar saga ok Heiðreks (The Saga of Hervör and Heidrek) Hlöðskviða (The Battle of the Goths and Huns) In Greco-Roman literature Ambrose. Ammianus Marcellinus The anonymous author(s) of the Augustan History Aurelius Victor: The Caesars, a history from Augustus to Constantius II Cassiodorus: A lost history of the Goths used by Jordanes Claudian: Poems Epitome de Caesaribus Eunapius" Eutropius: Breviary Eusebius George Syncellus Gregory of Nyssa Isidore of Seville in his History of the Kings of the Goths, Vandals, and Suevi Jerome: Chronicle Jordanes, in his Getica Julian the Apostate Lactantius: On the death of the Persecutors Olympiodorus of Thebes Panegyrici latini Paulinus the Deacon: Life of bishop Ambrose of Milan Paulus Orosius Philostorgius: Greek church history Pliny the Elder in Natural History Procopius Ptolemy in Geography Sozomen Strabo in Geographica Synesius: De regno and De providentia. Tacitus in Germania and Annals'' Themistius: Speeches Theoderet of Cyrrhus Theodosian Code Zosimus See also Gothic Wars Gaut Getae Gutes Geats Gothicism Gutian people Notes and sources Notes Ancient sources Modern sources Further reading Category:Early Germanic peoples
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Conventional clothes dryers include a rotating drum into which textiles to be dried are placed. The textiles are dried by forcing heated air through the wet laundry rotating within the drum. Moisture is removed along with the air exiting the dryer or via a condensed water duct. Conventional clothes dryers have been controlled in various ways. The simplest of these is a timer that controls the duration of the drying cycle. When using a timer, the user places wet laundry inside the dryer and selects the duration for the drying cycle. The dryer cycle then proceeds until the timer expires. Although this method is relatively simple, it is difficult to accurately estimate the length of time required to reach a desired final moisture level, or “dryness,” for every type of textile. If the cycle length is too short, the textiles will not be fully dry at the end of the cycle, and the user must initiate another dryer cycle to finish the drying process. If, on the other hand, the cycle length is too long, the clothes may become “overdry,” which may result in premature textile degradation and/or damage, excess energy consumption, and an associated increase in energy costs.
3.6875
4
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Raman spectroscopy is an optical spectroscopy technique, which measures the inelastic scattering, i.e. Raman scattering of monochromatic light by a material to produce a spectrum characteristic of the material. Raman spectroscopy has been demonstrated to be a powerful non-invasive analytical technology for material characterization and identification. Conventional Raman spectroscopy generally utilizes a well-focused laser beam to produce Raman scattering signal from the sample. This approach has the apparent advantage of relatively high efficiency in Raman signal excitation and collection. However, it also suffers from the following drawbacks. First, only a small volume of the sample is measured. Thus the collected Raman spectrum may not be very representative, especially for some non-uniform samples. Second, the tightly focused laser beam may cause damage to some delicate samples. Third, for diffusely scattering samples which are not transparent to the laser beam, this approach will only measure the Raman scattering signal from the surface layer of the sample. The majority of the material underneath the surface will be almost completely out of reach. There thus exists a need for an improved light delivery and collection device for performing Raman spectroscopy, which not only allows the measurement of a large area of the sample but also enables sub-surface Raman signal excitation and collection.
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[The outermost enamel layer. A comparative scanning electron microscopic study]. The surface of the enamel layer was scanned in teeth of some representative animal species. We studied the structural organization of enamel at the surface of the teeth and also in subsurface. The surface layer was often described as "aprismatic". But, nevertheless, in mammals, prisms often reach the surface. They are packed together almost perpendicular to the periphery. The term "aprismatic" seems inappropriate. But the surface layer is particular in both a structural, physical and chemical standpoint. Its distribution on the enamel surfaces explains the variability of the etching patterns from an area to another on the same tooth.
3.203125
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1. Field Example embodiments of the present invention relate to a nozzle plate including a protrusion type nozzle and a method of fabricating the nozzle plate. 2. Description of the Related Art Inkjet printing involves ejecting fine droplets of ink onto a printing medium using nozzles formed in a nozzle plate. Inkjet printing may be used to print a predetermined image by ejecting the fine droplets onto desired portions of the printing medium. Inkjet printing technology may be applied in various fields of printable electronics, biotechnology, and bioscience, as well as in the image printing field. For example, a flexible substrate, besides a glass substrate, may be used to fabricate electronic circuits, and thus, the inkjet printing technology may be applied in the field of flexible display apparatuses. According to inkjet printing, a pattern may be formed by just one process, and thus, processing costs may be lower than that of a conventional photolithography process. Inkjet printing technology may be classified into thermal type printing technology and piezoelectric type printing technology. In the thermal type printing technology, bubbles may be generated using a heat source and droplets may be ejected using an expansion property of the bubbles. The piezoelectric type printing technology ejects the droplets using a transformation of piezoelectric material. Electro-hydrodynamic type printing technology ejects droplets of ink by using an electrostatic force. The electro-hydrodynamic type printing technology has an advantage that a volume of an ejected droplet may be greatly reduced when compared with the conventional thermal type and the conventional piezoelectric type printing technologies.
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This invention relates to voltage reference circuits, and more particularly, to a bandgap voltage reference circuit for providing a stable output voltage operating independent of temperature and power supply variations. Voltage reference circuits are common in many modern electronic designs for providing a stable reference signal. The bandgap voltage reference circuit is well suited for this niche due to its temperature independent characteristics as discussed in an article entitled "A SIMPLE THREE-TERMINAL IC BANDGAP REFERENCE" by A. Paul Brokaw, IEEE Journal of Solid State Circuits, Vol. SC-9, No. 6, December, 1974. Briefly, the Brokaw article discloses a two transistor configuration conducting equal currents, but having dissimilar emitter areas, say eight-to-one, creating different current densities and base-emitter junction potentials (V.sub.be). The first transistor typically possesses the larger emitter area and, correspondingly, the lower current density and the lesser V.sub.be. By connecting two resistors in series with the emitter path of the first transistor and coupling the emitter of the second transistor to the interconnection thereof, a delta V.sub.be having a positive temperature coefficient is developed across the upper resistor. If the currents flowing through the first and second transistors are made of appropriate and constant magnitude and equal in value, the positive temperature coefficient of the voltage across the upper resistor tends to cancel the inherent negative temperature coefficient of the base-emitter junction of the first transistor thereby providing an output voltage at the collector of the second transistor which is insensitive to temperature variation, as is understood. The current flowing through the first and second transistors is typically provided by a PNP transistor current mirror configuration having the emitters thereof coupled to the positive power supply conductor. Any transients appearing on the positive power supply are reflected in the current flowing through the first and second transistors, inducing variation in the V.sub.be 's thereof and the potential developed across the emitter resistors. This translates to movement in the collector potential of the second transistor, thus, the output voltage is dependent upon the power supply voltage. The fluctuation in the circuit signal levels attributed to power supply variation is commonly known as the Early voltage effect and is an undesirable condition which adversely influences the regulated output signal. Hence, there is a need for an improved voltage reference circuit having an output voltage operating independent of temperature and power supply variations.
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It’s common for social animals to adopt and care for orphaned offspring. According to ScienceDaily, other loner species — like squirrels — may be learning such altruism. In yesterday’s Daily Briefing, MNN touched on this story saying, “A team of Canadian researchers have discovered squirrels will sometimes adopt related pups that have lost their mother, revealing a soft side of the arboreal rodents that scientists previously hadn't seen.” Evolutionary biologist and professor Andrew McAdam, from the University of Guelph in Ontario, Canada, along with researchers from the University of Alberta and McGill University were the scientists behind the study. McAdam said, “Red squirrels live in complete isolation and are very territorial. The only time they will allow another squirrel on their territory is the one day a year when the females are ready to mate or when they are nursing their pups.” Yet the study, published in Nature Communications, found that squirrels adopt orphaned pups if they are related … but even that is a rare occurrence. How rare? McAdam and his team found five cases of adoption in more than two decades of research. But ScienceDaily says, “Jamie Gorrell, a PhD candidate at the University of Alberta, identified 34 cases of potential adoption over 20 years. An adoption is possible only if the mother dies and a nearby squirrel is also nursing.” But even by that slightly higher standard, 34 cases out of the thousands of litters over the course of 20 years proves that the squirrels rarely adopt. According to McAdam, relatedness plays a critical role in the decision by a neighboring squirrel to adopt. In the five examples in his study, the pups were nieces, nephews, siblings, or grandchildren to the adoptive mother. "From an evolutionary perspective, the phenomenon of adoption raises the question of why an animal would adopt in the first place given that it jeopardizes the survival of their own offspring," said McAdam. "Under the right conditions, an animal can propagate more copies of its genes by helping relatives to raise their offspring than by producing offspring of their own. So in some cases it might be a good bet to adopt and accept these costs." McAdam found that squirrels only adopt when the orphans carry a large percentage of the same genes, meaning that they are more likely to adopt siblings, nieces, or nephews rather than more distant relatives. Amazingly enough, McAdam also noted that squirrels are able to assess which pups are related to them. Squirrels rarely interact with their neighbors, but an adoption may take place if they fail to hear the unique call of a nearby relative for several days, causing them to investigate. If they choose to take in the orphaned pups, they carry them back to their nest on their backs.
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Beavers are famous for their buckteeth and large, flat tails. These two well-known features aid beavers in their lives from day to day. The beaver’s teeth never stop growing. Chewing on tree trunks and branches helps keep the teeth from getting too long. A beaver’s front teeth stick out in front of their lips. That way, beavers can cut and chew underwater wood without getting water in their mouths. Beavers have a coating on their teeth that contains iron, which helps prevent tooth decay. A beaver’s paddle-shaped tail is black and scaly. In water, it functions like a boat rudder, helping steer the beaver as it moves logs to its dam. Beavers are builders! They spend much of their time building and maintaining their houses: dams and lodges—large dome-shaped piles of branches in lakes, rivers and larger streams. Beavers access their lodges through underwater entrances, which lead into dry living areas. As the colder months approach, they spread a thin layer of mud on top of the lodge to keep out any predators, such as lynx and wolves. If a beaver feels threatened, it will slap its tail on the surface of the water to warn other beavers in the area, then it will dive deep underwater to stay safe. Beavers can be found around lakes and streams all over Canada. In the past, beavers were over-hunted for their fur and meat, threatening the population. They have come back, however, thanks to wetland rehabilitation and other conservation efforts. Fast Facts: Beaver Scientific name: Castor canadensis Average size: 74 to 90 centimetres Average weight: Can weigh up to 32 kilograms Super Swimmers Beavers have clear membranes over their eyes that help them to see underwater, like goggles. Record Holder The world’s longest beaver dam is found in Alberta’s Wood Buffalo National Park and measures 850 metres. Dams usually average about 100 metres in length. National Symbol The beaver was made an official emblem of Canada in 1975 in recognition of the importance of the fur trade. Did you know? The beaver has long been an animal of importance to First Nations in North America, and beaver pelts formed the basis of trade with European settlers starting in the 1530s.
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Introduction {#s1} ============ A phylogenetic tree of a group of species (taxa) describes the evolutionary relationship among the species. The study of phylogeny not only helps to identify the historical relationships among a group of organisms, but also supports some other biological research such as drug and vaccine design, protein structure prediction, multiple sequence alignment and so on [@pone.0104008-Linder1]. The ultimate goal of this research community is to infer the *Tree of Life*, the phylogeny of all living organisms on earth, provided that it exists. Phylogenetic tree reconstruction by analyzing the molecular sequences of different species can be regarded as the *sequence-based* reconstruction of the phylogeny. Sequence-based phylogenetic methods are basically of three types [@pone.0104008-Linder1]: (a) distance-based methods, such as Neighbor Joining (NJ) [@pone.0104008-Saitou1], which has very fast practical performance; (b) heuristics for either Maximum-Likelihood (ML) [@pone.0104008-Felsenstein1] or Maximum-Parsimony (MP) [@pone.0104008-Fitch1], which are two NP hard optimization problems; and (c) the Bayesian Markov Chain Monte Carlo (MCMC) method, which, instead of a single tree, produces a probability distribution of the trees or aspects of the evolutionary history. Sequence-based methods are generally highly accurate. However, these methods are computationally intensive. As a result, these can only be applied on small to moderate sized datasets if we want to provide results having an acceptable level of accuracy within a moderate amount of time. For larger datasets (few hundreds of taxa (species)), these methods may need several weeks or months to provide results with an acceptable level of accuracy [@pone.0104008-Linder1]. As the amount of molecular data is accumulating exponentially with the continuous advancement in sequencing technologies, scientists are facing new computational challenges to analyze these enormous amount of data. Therefore, we are forced to rely on *supertree* methods, where smaller trees on overlapping groups of species are combined together to get a single larger tree. Supertree-based tree construction is a two-phase method: in the first phase, many small trees on overlapping subsets of taxa are constructed using a sequence-based method; and in the next phase the small trees are summarized into a complete tree over the full set of taxa. Supertree methods are considered to be the likely solutions towards assembling the *Tree of Life*. Hence, these methods have drawn potential research interest in recent years. Supertree methods have two major motivations: firstly, it gives us the opportunity to achieve increased scalability and secondly, it is more suitable to combine the phylogenetic analyses on different types of data (e.g., molecular, morphological and gene-order data) or species groups. The careful design of supertree methods may allow us to work on very large (several hundreds taxa) datasets more accurately and easily. The most widely used supertree method is called the Matrix Representation with Parsimony (MRP) [@pone.0104008-Baum1], [@pone.0104008-Regan1]. MRP encodes all the small trees into a matrix using the characters , and . Then it uses Maximum-Parsimony (MP) [@pone.0104008-Fitch1] to get a tree from the data matrix. MRP is considered to be the most reliable supertree method to date. But since it uses an NP hard problem to analyze the data matrix, it is not efficient for large datasets. *Quartet amalgamation* methods are supertree methods when each of the the small trees to be combined is a quatret, i.e., an unrooted tree having taxa. Quartet is the most basic piece of unrooted phylogenetic information. Quartet-based phylogenetic inference has drawn significant attention from the research community, and numerous quartet-based methods have been developed over the last two decades. In this paper, we present a novel and highly accurate quartet amalgamation technique. We conduct an extensive experimental study that demonstrates the superiority of our algorithm over QMC [@pone.0104008-Snir1]--[@pone.0104008-Snir3], which is known as the best quartet amalgamation method to date. With the increasing abundance of molecular data, constructing species trees from multilocus data has become the focus of attention. But combining data on multiple loci is not a trivial task due to the gene tree discordance [@pone.0104008-Maddison1]--[@pone.0104008-Pamilo1]. The task is even more complicated with the striking recognition that the most probable rooted gene tree topology (under a coalescent model [@pone.0104008-Pamilo1]--[@pone.0104008-Harding1]) need not match the species tree topology [@pone.0104008-Degnan2], [@pone.0104008-Degnan3]. These are termed as *Anomalous gene trees* (AGTs). AGTs occur because not all tree topologies are equiprobable under the coalescent model [@pone.0104008-Harding1], [@pone.0104008-Brown1], [@pone.0104008-Steel1]. In fact, rooted AGTs exist for any species tree with or more taxa. It has also been shown that rooted AGTs cannot occur with a three taxa and a symmetric four taxa species tree [@pone.0104008-Degnan2]. AGTs have also been studied for unrooted gene trees, and it has been observed that for a species tree with four taxa, the most probable rooted gene tree topologies have the same unrooted topology as the species tree [@pone.0104008-Degnan4]. This observation indicates that the most frequently occurring unrooted quartet is a consistent estimate of the unrooted species tree [@pone.0104008-Degnan4]. Thus, quartet based phylogeny can offer a sensible and statistically consistent approach to combine multilocus data, despite gene tree incongruence and AGTs [@pone.0104008-Larget1], . Thus a highly accurate quartet amalgamation approach will help to design species tree estimation methods that are not susceptible to the gene tree discordance and AGTs. Notably, as has already been mentioned above, the other important advantage of quartet-based methods is that efficient design of such inference algorithm can be scalable to very large datasets (several hundreds or thousands of taxa). Previous Works {#s1a} -------------- Quartet-based phylogenetic tree reconstruction has been receiving extensive attention in the literature for more than two decades. Different approaches have been proposed and improved time to time. Among these, the most prominent approaches are, quartet puzzling (QP), quartet joining (QJ) and quartet max-cut (QMC). Quartet puzzling (QP) [@pone.0104008-Strimmer1] infers the phylogeny of sequences using a weighting mechanism. First, it computes the maximum-likelihood values for the three topologies on every 4 taxa and uses these values to compute the corresponding probabilities. Using these probabilities as weights, the puzzling step constructs a collection of trees over taxa. Finally it returns a consensus tree over *n*-taxa. TREE-PUZZLE [@pone.0104008-Schmidt1] is a widely used program package that implements QP. In 1997, Strimmer et al. [@pone.0104008-Strimmer2] extended the original QP algorithm by proposing three different weighting schemes, namely, continuous, binary and discrete. Later in 2001, Ranwez and Gascuel [@pone.0104008-Ranwez1] proposed weight optimization (WO), an algorithm which is also based on weighted 4-trees inferred by using the maximum likelihood approach. WO uses the continuous weighting scheme defined in [@pone.0104008-Strimmer2] and it searches for a tree on taxa such that the sum of the weights of the 4-trees induced by this tree is maximal [@pone.0104008-Ranwez1]. Unlike QP, WO constructs a single tree over taxa; hence no consensus step is required. Though the speed and accuracy of WO are better than that of QP, its accuracy is lower than that of the methods based on evolutionary distances or maximum likelihood. Quartet joining (QJ) [@pone.0104008-Xin1] was introduced in 2007 to overcome the limitations of QP and WO in outperforming the distance based methods. QJ provides the theoretical guarantee to generate the accurate tree if a complete set of consistent quartets is present. On average QJ outperforms QP and its performance is very close to the performance of NJ [@pone.0104008-Saitou1], but QJ outperforms NJ on quartet sets with low quartet consistency rate [@pone.0104008-Xin1]. In 2008, Snir et al. [@pone.0104008-Snir1] proposed a new quartet-based method, *short quartet puzzling* (SQP). The experimental studies in [@pone.0104008-Snir1] shows that SQP provides more accurate trees than QP, NJ and MP. It differs from the previous techniques in that it does not require all three topologies of the quartets on every 4 taxa. It is able to construct the output tree from a subset of all possible quartets as input. This is a two-phase technique: the first phase uses the randomized technique for selecting input quartets from all possible 4-trees (estimated using ML), and the second phase uses Quartet Max Cut (QMC) [@pone.0104008-Snir1], [@pone.0104008-Snir2] technique for combining quartets into a single tree. The experimental study conducted by Swenson et al. [@pone.0104008-Swenson1] concludes that QMC performs better than the other supertree methods and MRP for smaller (100-taxon and 500-taxon) and high scaffold (i.e., high scaffold density) datasets. But MRP outperforms QMC and other supertree methods on larger and low scaffold (i.e., low scaffold density) datasets [@pone.0104008-Swenson1]. Subsequently, Snir and Rao presented a fast and scalable implementation of QMC [@pone.0104008-Snir3], where they reported the improvement of QMC over MRP in terms of accuracy and running time. Although MRP is the mostly used supertree method in practice, the studies of [@pone.0104008-Snir3], [@pone.0104008-Swenson1] suggest that QMC is so far the best quartet-based supertree method. In this paper, we present a new quartet-based phylogeny reconstruction algorithm, *Quartet FM* (QFM), which uses a bipartition technique inspired from the famous Fiduccia and Mattheyses (FM) algorithm for bipartitioning a hyper graph minimizing the cut size [@pone.0104008-Fiduccia1]. As will be reported later, QFM is highly accurate and scalable to large datasets (upto several hundreds of taxa). We demonstrate the accuracy of QFM by analyzing its performance on both simulated and biological datasets. We have compared our method on simulated datasets with Quartet MaxCut (QMC) [@pone.0104008-Snir1]--[@pone.0104008-Snir3], and showed the superiority of our method over QMC in terms of the accuracy of the estimated trees. To show the potential of our method, we also analyzed a real biological dataset containing species from genera of birds (*Amytornis*, *Stipiturus*, *Malurus* and *Clytomias*). We have demonstrated a qualitative analysis of our results on real dataset based on the results of some rigorous previous studies on the same dataset. Problem Definition {#s1b} ------------------ We address the problem of *Maximum Quartet Consistency* (MQC), which is a natural optimization problem. This problem takes a quartet set as the input and finds a phylogenetic tree such that the *maximum* number of quartets in become "consistent" with (or "satisfies" the maximum number of quartets). Now we formally define the problem. Problem 1 Maximum Quartet Consistency {#s1c} ------------------------------------- ***Input:*** *A multiset of quartets* *on a taxa set* . ***Output:*** *A phylogenetic tree* *on* *such that* *satisfies the maximum number of quartets of* . The Maximum Quartet Consistency (MQC) problem is an NP-hard optimization problem [@pone.0104008-Steel2]. Both exact and heuristic approaches are available for the MQC problem in the literature [@pone.0104008-Morgado1]. The running time of an exact algorithm grows exponentially with the increase of number of taxa, since the number of possible trees grows more than exponentially with the number of taxa [@pone.0104008-Hodkinson1]. So for larger datasets we have to resort to the heuristic solutions. The focus of this work is on heuristic solutions for the MQC problem as we aim to build the phylogenetic tree for several hundreds of taxa. Results {#s2} ======= We have conducted an extensive experimental study on both simulated and biological datasets. We have evaluated the accuracy of the trees estimated by QFM and compared the results to that of QMC [@pone.0104008-Snir3]. QMC is the most accurate quartet amalgamation method developed to date, and was shown to be more accurate than MRP [@pone.0104008-Snir3]. We have reported RF (Robinson Foulds) [@pone.0104008-Robinson1] rates of the estimated trees. RF rate is the mostly used error metric, which is the ratio of the sum of the number of false positive and false negative edges to a factor , where is the number of taxa [@pone.0104008-Linder1]. The false positive (FP) and false negative (FN) edges are respectively, the edges which are absent in the true tree but present in the estimated tree, and the edges which are present in the true tree but absent in the estimated tree. Simulated Datasets {#s2a} ------------------ To investigate the performance of our method on various model conditions, we have generated quartet sets, taken uniformly at random from model trees, by varying the number of taxa (), the number of quartets () and the percentage of consistent quartets () with respect to the model tree ( consistency level means that quartets are flipped to disagree with the model tree). We have generated model species trees with , , , , , and taxa. To generate the model trees and the input quartet sets, we have used the tool developed and used in [@pone.0104008-Snir3]. The tool takes as input the number of taxa (), number of quartets () and the consistency level (), and returns the quartet sets accordingly. For , , , we have generated , and quartets. We have not generated more quartets because quartets have been empirically shown to be enough to construct very accurate phylogenetic trees [@pone.0104008-Snir3]. Although is a small number, we have chosen this size to test the performance of both methods on a comparatively smaller number of quartets as well. For , , and -taxon model trees, we have generated datasets with and . For each size (), we have varied the percentage of consistent quartets () by making it , , , and . Thus in total we have generated model conditions. To test the statistical robustness, we have generated replicates of data for each of these model conditions. For each model condition, we report the average RF rate over the replicates of data. We also report the standard error, given by where is the standard deviation and is the number of datapoints (which is in our experiments). The standard errors are reported in Table S1 and Table S2 in [File S1](#pone.0104008.s001){ref-type="supplementary-material"}. We have used Wilcoxon signed-rank test with to test the statistical significance of the differences between QFM and QMC. The results of the Wilcoxon T-test (*p*-values) are reported in Table S3 in [File S1](#pone.0104008.s001){ref-type="supplementary-material"}. Analyses on the Simulated Datasets {#s2b} ---------------------------------- We now present the results on the simulated datasets mentioned above. In each case, we have compared the average RF rate for the trees estimated by QFM and QMC. The results for , , and are summarized in [Table 1](#pone-0104008-t001){ref-type="table"}. [Figure 1](#pone-0104008-g001){ref-type="fig"} shows the bar charts comparing the values presented in [Table 1](#pone-0104008-t001){ref-type="table"}. The results in [Table 1](#pone-0104008-t001){ref-type="table"} is presented in batches for different values of as follows. For , , , we have three rows, one each for , and . For , , , we have two rows, one each for and . The topmost row of each batch of [Table 1](#pone-0104008-t001){ref-type="table"} shows the results when (from left to right, the consistency levels reported are , , , , respectively). For this () case, both QMC and QFM have performed poorly which implies that quartets are quite insufficient for accurate phylogeny reconstruction. This can be attributed to the fact that is a very small number compared to (i.e., the possible number of quartets). However, as the consistency level () increases, QFM starts to produce better trees than QMC; and very often the improvements of QFM over QMC are statistically significant (see Table S3 in [File S1](#pone.0104008.s001){ref-type="supplementary-material"}). This is very promising in the sense that, QFM can construct more accurate trees than QMC even with very small number of quartets. The second row of each batch of [Table 1](#pone-0104008-t001){ref-type="table"} shows the results with quartets. With quartets, both QFM and QMC begin to produce better trees than that of quartets. However, quadratic number of quartets is still not sufficient for reconstructing an accurate tree (which confirms the observation of [@pone.0104008-Snir3]). But as before, QFM is statistically significantly better than QMC in most of the cases. The bottom most row of the first three batches in [Table 1](#pone-0104008-t001){ref-type="table"} shows the results with quartets. In this case, both QFM and QMC reconstruct highly accurate species trees (error rates are close to zero) even with consistent quartets. ![Average RF rates of QFM and QMC on the simulated datasets.\ We show average RF rates (over 20 replicates of data) for each model condition. We varied the number of taxa (), number of quartets () and the percentage of consistency level (). For a particular value of and , the number of taxa is varied along the X-axis, the average RF rate is shown along the Y-axis, and the error bars represent the standard errors. From left to right: the number of quartets are , , and . From top to bottom: 70%, 80%, 90% and 95% of the input quartets are consistent with the model species tree. We did not run our method on quartets when the number of taxa is more than , since these are computationally intensive and QFM could not be run within a reasonable time limit. Moreover, these model conditions are less revealing and interesting since both QMC and QFM can reconstruct the true species trees with quartets.](pone.0104008.g001){#pone-0104008-g001} 10.1371/journal.pone.0104008.t001 ###### Comparison of QFM and QMC under various model conditions. ![](pone.0104008.t001){#pone-0104008-t001-1} Average RF rate ----- -------- ----------------- ----------- ----------- ----------- ----------- ----------- ----------- ----------- 25 125 0.882 0.881 **0.739** **0.772** 0.577 0.577 **0.458** **0.468** 25 625 **0.272** **0.308** **0.155** **0.178** **0.073** **0.101** **0.051** **0.062** 25 8208 0 **0.002** 0 **0.002** 0 0 0 0 50 354 0.973 0.964 **0.890** **0.904** 0.757 0.756 **0.696** **0.709** 50 2500 **0.400** **0.426** **0.289** **0.344** **0.171** **0.184** **0.161** **0.174** 50 57164 **0.007** **0.011** 0 0 0 0 0 0 100 1000 **0.991** **0.993** **0.921** **0.937** **0.862** **0.866** **0.806** **0.822** 100 10000 **0.551** **0.597** **0.433** **0.454** **0.350** **0.365** **0.293** **0.308** 100 398108 **0.009** **0.010** **0.003** **0.004** 0.001 0.001 **0** **0.001** 200 2829 0.997 0.994 **0.955** **0.963** **0.909** **0.934** **0.887** **0.901** 200 40000 **0.695** **0.720** **0.585** **0.608** **0.488** **0.514** **0.450** **0.471** 300 5197 0.996 0.996 **0.965** **0.972** **0.921** **0.949** **0.907** **0.930** 300 90000 **0.752** **0.766** **0.655** **0.676** **0.561** **0.583** **0.526** **0.535** 400 8000 **0.993** **0.996** **0.963** **0.977** **0.926** **0.952** **0.923** **0.941** 400 160000 **0.786** **0.804** **0.707** **0.731** **0.624** **0.634** **0.590** **0.601** 500 11181 0.994 0.993 **0.967** **0.978** **0.938** **0.962** **0.926** **0.950** 500 250000 **0.813** **0.832** **0.736** **0.762** **0.663** **0.684** **0.616** **0.636** Average RF rates of QFM and QMC over the replicates of data under various model conditions. We varied the number of taxa (), the number of quartets (), and the percentage of consistent quartets (). Results are shown in bold face where QFM is better than QMC. From these results, it is clear that QFM either matches the accuracy of QMC or (in most cases) produces better trees than QMC. QFM outperforms QMC in cases out of the model conditions shown in [Table 1](#pone-0104008-t001){ref-type="table"}, and in cases the differences are statistically significant (see Table S3 in [File S1](#pone.0104008.s001){ref-type="supplementary-material"}). QMC is better than QFM on only cases, but the differences between the two methods are not statistically significant. For the rest cases, both QFM and QMC have equal error rates (these are mostly the datasets with quartets where both of them have been able to reconstruct the true trees). We have also evaluated QFM and QMC on the noise-free model conditions, meaning that all the quartets are accurate (). [Table 2](#pone-0104008-t002){ref-type="table"} demonstrates the results under the parameters () with . Of the model conditions analyzed, QFM has been found to be better than QMC on cases, and the improvements are statistically significant in cases (see Table S3 in [File S1](#pone.0104008.s001){ref-type="supplementary-material"}). QMC is better than QFM in two cases but the differences are not statistically significant. In cases QFM and QMC have identical accuracy. 10.1371/journal.pone.0104008.t002 ###### Comparison of QFM and QMC under the noise-free model conditions. ![](pone.0104008.t002){#pone-0104008-t002-2} Average RF rate ----- -------- ----------------- ----------- 25 125 **0.444** **0.515** 25 625 0.056 0.052 25 8208 0 0 50 354 **0.661** **0.666** 50 2500 0.140 0.140 50 57164 0 0 100 1000 **0.777** **0.797** 100 10000 **0.269** **0.274** 100 398108 0 0 200 2829 **0.848** **0.881** 200 40000 0.424 0.424 300 5197 **0.887** **0.907** 300 90000 0.506 0.499 400 8000 **0.897** **0.930** 400 160000 **0.554** **0.555** 500 11181 **0.903** **0.937** 500 250000 **0.590** **0.606** Average RF rates of QFM and QMC over the replicates of data under the noise-free model conditions (). We varied the number of taxa () and the number of quartets (). Results are shown in bold face where QFM is better than QMC. Computational Issues {#s2c} -------------------- We have evaluated the running time and memory usage of QFM and QMC. On smaller datasets, both QFM and QMC run in few seconds. For example, on taxa, QFM took between seconds to seconds (depending on the number of quartets), and QMC took less than seconds. Both of these methods are very fast on the datasets with up to taxa and with quartets: QFM took few minutes while QMC completed in few seconds. However, QFM is much slower than QMC on the larger datasets. For example, QFM took hours for the largest datasets of our experiment with taxa and quartets, while QMC took only one minute. We believe that this difference is due to the naive implementation of our algorithm. QMC has been implemented in a very efficient code, and it scales well on larger datasets. We are currently working on improving our implementation using advanced data structures. We are also parallelizing our divide and conquer based approach. We have also measured the memory usage by these methods. Both QFM and QMC are memory efficient and use only few megabytes of memory. For example, the peak memory usages by QMC and QFM on the datasets with taxa and quartets are MB and MB, respectively. Analyses on the Avian Biological Dataset (Australo-Papuan Fairy-wrens) {#s2d} ---------------------------------------------------------------------- We have further evaluated the performance of QFM on a real avian biological dataset consisting of birds. Since Avian phylogeny is considered to be hard to reconstruct, we have chosen this dataset as a good representative of real datasets. This dataset consists of gene trees on species representing genera of birds (*Amytornis*, *Stipiturus*, *Malurus* and *Clytomias*) from Australo-Papuan avian family Maluridae, obtained from TreeBASE [@pone.0104008-Sanderson1]. This dataset has originally been used to study the efficacy of species tree methods at the family level in birds, using the Australo-Papuan Fairy-wrens (Passeriformes: Maluridae) clade [@pone.0104008-Lee1]. Due to the presence of substantial amount of incomplete lineage sorting (ILS) [@pone.0104008-Lee1], analyzing this family of birds is quite challenging. We have decomposed every gene tree into its induced quartets which is called *embedded quartets* [@pone.0104008-Snir3], [@pone.0104008-Zhaxybayeva1]. Then, we have taken the union of all these quartets (multiple copies of a quartet have been retained). In this way we get 227,700 quartets. We have used these quartets to estimate a species tree using our method (QFM). We also ran QMC on this datasets. Both QFM and QMC returned the same tree. The tree is shown in [Figure 2](#pone-0104008-g002){ref-type="fig"}. ![The 25 species avian phylogeny, representing 4 genera of birds from Maluridae family, estimated by QFM using the 227,700 embedded quartets in 18 gene trees.\ The evolutionary relationships maintained by this tree are supported by the findings of the previous studies [@pone.0104008-Lee1], [@pone.0104008-Christidis1], [@pone.0104008-Christidis2], [@pone.0104008-Donnellan1].](pone.0104008.g002){#pone-0104008-g002} Since we do not know the true trees for biological datasets, we have compared the result obtained from QFM with biological beliefs and other rigorous analyses. The tree returned by QFM (which is identical to the tree estimated by QMC) is quite interesting and consistent with the previous findings as discussed below. • QFM has been able to correctly identify the clusters associated with the four genera of birds. Also, it has placed the group of *Amytornis* birds as the sister to the rest of the family, and the group of *Stipiturus* birds as the sister to *Malurus* and *Clytomias* birds. These evolutionary relationships maintained by QFM are supported by the findings of the previous studies [@pone.0104008-Lee1], [@pone.0104008-Christidis1], [@pone.0104008-Christidis2]. • *Amytornis*: Using allozyme analysis, Christidis [@pone.0104008-Christidis2] has shown that *A. barbatus* is the earliest diverged lineage in the Amytornis genus. Same results have been obtained by a DNA sequencing study in [@pone.0104008-Christidis3]. The sequence-based analysis of Lee et al. [@pone.0104008-Lee1] also have confirmed this. Our analyses with QFM also have found the same pattern. Lee et al. [@pone.0104008-Lee1] also have shown that *A. housei* should be within the *textilis* complex, which is confirmed by our QFM tree. • *Stipiturus*: Evolutionary relationships within the *Stipiturus* genus have been well studied [@pone.0104008-Lee1], [@pone.0104008-Christidis1], [@pone.0104008-Donnellan1]. Our study is consistent with the previous findings: *S. mallee* and *S. ruficeps* are closer to each other than they are to *S. malachurus*. • *Clytomyias* and *Malurus*: *C. insignis* was placed to *Stipiturus* species by [@pone.0104008-Christidis1]. However, in a more recent extensive multi-locus study, Lee et al. [@pone.0104008-Lee1] argued that *C. insignis* is closer to *M. grayi*. Our study has also confirmed this fact. Also our study has confirmed their [@pone.0104008-Lee1] findings that *M. alboscapulatus* is closer to *M. melanocephalus* than to *M. leucopterus*. Lee *et al.* [@pone.0104008-Lee1] showed that ILS is likely a general feature of the genetic history of these avian species. Since quartets are not prone to anomaly zone [@pone.0104008-Degnan2], [@pone.0104008-Degnan4], quartet based analyses to resolve the avian history is of high importance. Interestingly, both QMC and QFM resolved the evolutionary history of these birds similarly. Therefore, we believe that this tree should be considered as a reasonable hypothesis about the evolutionary history of this family of birds. Discussion {#s3} ========== In this work we have presented a novel and highly accurate quartet amalgamation technique, which we refer to as QFM. We have demonstrated the superiority of our method over QMC, which is known to be the best quartet amalgamation method to date. QFM is a new promising divide and conquer supertree method having an algorithmic appeal. We have conducted an extensive experimental study comparing QFM against QMC under different model conditions by varying different parameters. For almost all model conditions considered, QFM performs at least equal but in most cases better than QMC. In line with the experimental results shown in [@pone.0104008-Snir3], we have found that quadratic sampling of quartets is not sufficient for accurate supertree construction. However, with quartets, both QFM and QMC can reconstruct very accurate trees indicating that it is possible to reconstruct an accurate supertree from large number of quartets, even with high amount of noise in the input data. QFM has also been tested on real biological datasets and has been shown to perform pretty well. The tree estimated by QFM has maintained the important evolutionary relationships despite the presence of incomplete lineage sorting. This is particularly interesting because this suggests that we can use quartet-based technique to develop species tree estimation method (from multi-locus data), which is less susceptible to gene tree incongruence due to ILS. Species tree estimation is frequently based on phylogenomic approaches that use multiple genes from throughout the genome. However, combining data on multiple genes is not a trivial task. Genes evolve through biological processes that include deep coalescence (also known as incomplete lineage sorting (ILS)), duplication and loss, horizontal gene transfer etc. As a result the individual gene histories can differ from each other [@pone.0104008-Maddison1]. Species tree estimation in the presence of ILS is a challenging task. Moreover, anomalous gene trees (AGTs) make this task even more complicated [@pone.0104008-Degnan2], [@pone.0104008-Degnan3]. It has been proven that AGTs cannot occur in quartets and thus the most probable quartets induced by the true gene trees represent the true species trees for the corresponding four species [@pone.0104008-Degnan2], [@pone.0104008-Degnan4], Therefore, quartets can be used to design statistically consistent methods (methods that have the statistical guarantee to construct the true species tree given sufficiently large number of true gene trees) for constructing the species tree from gene trees (which evolve with ILS) as follows. First, we compute the quartets induced by the gene trees. For every four species, there are three possible quartets. Given sufficiently large number of true gene trees, the most probable quartets (the most frequently occurring quartets) on every four species represent the true species trees for those four species. Thus combining the most probable quartets to get a single and coherent species tree is an statistically consistent approach for species tree estimation. In this context, we can formalize the maximum weighted quartet satisfiability problem as follows. • ***Input:*** A set of weighted quartets. • ***Output:*** The species tree such that maximizes the summation of the weights of the satisfied quartets in . We can define the weight of a quartet as the proportion of the gene trees that induce . We can also incorporate the branch lengths in defining the weights. One major advantage of QFM is that it can readily be adapted to take a set of weighted quartets as input without making any change in its algorithmic constructs. Therefore, we think QFM is an important contribution to the phylogenomic analyses, in particular for estimating species trees from a set of gene trees where gene trees can be discordant from each other due to ILS. Another advantage of QFM lies in its flexibility in choosing the *partition score* function (see "Partition Score" section). QFM can be customized to take different scoring functions (i.e., , , etc.) without making any change in the algorithmic construct. We have observed that QFM may not give the same result for different scoring functions for the same dataset. So for different datasets, we may obtain better results by adapting different suitable scoring functions. Thus QFM provides us with the flexibility to change the scoring function as needed. In future we shall try to make our algorithm self-adaptable to the appropriate scoring function by analyzing different characteristics of the input datasets. Notably, as has already been discussed above, one shortcoming of the current implementation of QFM is that it is not as fast as QMC. Materials and Methods {#s4} ===================== In this section we present our heuristic algorithm, namely, the **Q**uartet **FM** (**QFM**) algorithm. Our algorithm employs a *quartet based supertree reconstruction* technique that involves a bipartition method inspired by the Fiduccia Mattheyses (FM) bipartition technique [@pone.0104008-Fiduccia1]. Basics {#s4a} ------ A quartet is *consistent* with a tree if in , there is an edge (or path in general) separating and from and . For any four taxa, only one quartet (out of possible quartets) will be consistent with a tree . In [Figure 3](#pone-0104008-g003){ref-type="fig"} among the three quartets, quartet is consistent with tree as there exists an edge in such that it separates and from and . Other two quartets are inconsistent with as no such edge exists in . ![Quartet consistency with a tree .\ Among the three quartets, only  =  ((, ), (,)) is consistent with because has an internal edge that separates taxa and from taxa and in .](pone.0104008.g003){#pone-0104008-g003} A bipartition of an unrooted tree is formed by taking any edge in , and writing down the two sets of taxa that would be formed by deleting that edge. Let be a tree over the taxa set . Now, if we take an internal edge of and delete , then we get two subtrees, namely, and . Let and be the sets of taxa of and respectively. We shall denote such bipartition by (, ). Thus an internal edge in corresponds to a bipartition of . A quartet is *satisfied* with respect to a bipartition if taxa and reside in one part and taxa and reside in the other. A *satisfied* quartet is *consistent* with . The quartet is said to be *violated* with respect to a bipartition when taxa and (or and ) reside in one part and taxa and (or and ) reside in the other part. On the other hand, is said to be *deferred* with respect to a bipartition if any three of its four taxa reside in one part and the fourth one resides in the other. A tree over a taxa set is said to be a *star*, if has only one internal node and there is an edge from the internal node incident to each taxon . We shall refer to such a tree as a *depth one tree*. Divide and conquer approach {#s4b} --------------------------- We follow a divide and conquer approach similar to QMC [@pone.0104008-Snir1]--[@pone.0104008-Snir3]. Let, be a set of quartets over a set of taxa, . We aim to construct a tree on , satisfying the largest number of input quartets possible. The divide and conquer approach recursively creates bipartition of the taxa set, where each bipartition corresponds to an internal edge in the tree under construction. QMC uses a heuristic bipartition technique which is based on finding a maximum cut (MaxCut) in a graph over the taxa set, where the edges represent the input quartets [@pone.0104008-Snir3]. On the other hand, our algorithm uses a heuristic bipartition algorithm inspired by the famous Fiduccia and Mattheyses (FM) [@pone.0104008-Fiduccia1] bipartition algorithm. ### Divide {#s4b1} At each recursive step, we partition the taxa set into two sets and . We shall describe the bipartitioning algorithm in "Method of Bipartition" section. After the algorithm partitions the taxa set, it augments both parts ( and ) with a unique dummy (artificial) taxon. This taxon will play a role while returning from the recursion. After the addition of the dummy taxon to the sets and , we subdivide the quartet set into two sets, and . A quartet set takes those quartets from such that either all four taxa , , and or any three thereof belong to (here ). In other words, satisfied or violated quartets with respect to the partition are not considered to be included in either or . Moreover, in every deferred quartet, where three taxa are in the same part, the other taxon is renamed by the name of the dummy taxon, and the quartet continues to the next step. Thus we get, two pairs: and . We then recurse on both pairs and if is non-empty and . If either is empty or , we return a *depth one tree* over the taxa set . ### Conquer {#s4b2} On returning from the recursion, at each step, we have two trees, (corresponding to ) and (corresponding to ). These two trees are rerooted at the dummy taxon. Then the dummy taxon is removed from each tree and the two roots are joined by an internal edge. [Figure 4](#pone-0104008-g004){ref-type="fig"} describes the high level divide and conquer algorithm. Let be the input quartet set and be the corresponding taxa set. Assume that  =  , , , , , , and hence . First, is partitioned into two sets, and by using the bipartition technique described in "Method of Bipartition" section. Here, is the dummy taxon. The bipartition satisfies quartets , and from . So these quartets will not be considered in the next level. takes and as three of the taxa of and reside in . We replace the taxon which does not belong to with the dummy taxon . Hence we get . Similarly we get . Next we recurse on and , and and are partitioned further into and , respectively. The partition satisfies and violates in and satisfies the only quartet in . So the quartet sets for the next level are empty and hence no more recursion is required. We return a *depth one tree* for each of the taxa sets , , and . The returned trees are merged by removing the dummy taxon of that level and joining the branches of the dummy taxa. In [Figure 4](#pone-0104008-g004){ref-type="fig"}, the upper half shows the *divide* steps. The *depth one trees* are returned when no more recursion is required. The lower half of [Figure 4](#pone-0104008-g004){ref-type="fig"} shows how the trees are returned and merged as the recursion unfolds (conquer step). Thus we get the final merged tree (shown at the bottom of [Figure 4](#pone-0104008-g004){ref-type="fig"}) satisfying quartets in total. The satisfied quartets are , , , and . ![Divide and conquer approach.\ Divide: At each step, the input set of taxa of this step is partitioned into two sets and an unique dummy taxon is added to both sets. The input quartet set is then partitioned into two sets according to the bipartition of the set of taxa. So we get two (taxa set, quartet set) pairs, which are input to the successive divide steps. If at any step, the quartet set gets empty or the size of the taxa set becomes less than or equal to , a depth one tree over the taxa set is returned. Conquer: At each step, there are two trees corresponding to the divide calls initiated at this step. These two trees are joined on the dummy taxon introduced at this step during divide. For example, the leftmost two depth one trees, when returned to its caller, are joined on the dummy taxon .](pone.0104008.g004){#pone-0104008-g004} Method of Bipartition {#s4c} --------------------- The most crucial part of our algorithm is the bipartition (divide step) technique. Here, we differ from QMC [@pone.0104008-Snir1]--[@pone.0104008-Snir3] and adopt a new bipartition technique inspired by the famous Fiduccia and Mattheyses (FM) algorithm for bipartitioning a hyper graph minimizing the cut size [@pone.0104008-Fiduccia1]. In divide and conquer based phylogenetic tree construction, the bipartition of the taxa set corresponds to an internal edge of the tree under construction. An internal edge, in turn, plays a role to make quartets to be satisfied or violated against the bipartition. So we adopt a different bipartition technique from that used in QMC, with an objective to get better results. Our bipartition algorithm takes a pair of taxa set and a quartet set (, ) as input. It partitions into two sets, namely, and with an objective that (, ) satisfies the maximum number of quartets from . The algorithm starts with an initial partition and iteratively searches for a better partition. We will use a heuristic search to find the best partition. Before we describe the steps of the algorithm, we describe the algorithmic components. ### Partition Score {#s4c1} We assess the quality of a partition by assigning a *partition score*. We use a scoring function, , such that the higher score will indicate a better partition. This function checks each against the partition and determines whether is *satisfied*, *violated* or *deferred*. We define the score function in terms of the number of satisfied and violated quartets. Let and denote the number of satisfied and violated quartets. Then, two natural ways of defining the score function are: 1) taking the difference between the number of satisfied and violated quartets (), and 2) taking the ratio of the number of satisfied and violated quartets (). As num In this paper, we used as the score function. We can also use some other complicated score functions defined in terms of the number of satisfied, violated and deferred quartets (i.e., , where denotes the number of deferred quartets). In our preliminary experimental study, we have explored different score functions and observed that gives better performance in most of the cases. Notably, although in some cases other functions (e.g., , ) achieve better results than (results are not shown in this paper), none of them is consistently better than . ### Gain Measure {#s4c2} Let be a partition of set of taxa . Let be a taxon and without loss of generality we assume that . Let be the partition after moving the taxa from to . That means, , and . Then we define the *gain* of the transfer of the taxon with respect to , denoted by *Gain* , as . ### Singleton Bipartition {#s4c3} A bipartition () of is *singleton* if or . In our bipartition algorithm, we keep a check for the singleton bipartition. We do not allow our bipartition algorithm to return a singleton bipartition to avoid the risk of an infinite loop. ### Algorithm {#s4c4} Now we describe the bipartition algorithm which we call MFM (Modified FM) Bipartition Algorithm. Let, (, ) be the input to the bipartition algorithm, where be a set of taxa and be a set of quartets over the taxa set . We start with an initial bipartition of . The initial bipartitioning is done in four steps. • Step 1: We count the frequency of each distinct quartet in . • Step 2: We then sort by the frequency count of the quartets in a decreasing order. • Step 3: Suppose after sorting , where . Now we consider the quartets one by one in the sorted order. Initially both and are empty. Let be a quartet in . If none of the taxa belongs to either or , then we insert and in and and in . Otherwise, if any of the taxa exists in either or we take the following actions to insert a taxon which doest not exist in or . We maintain an insertion order. We consider , , and respectively. -- To insert , we look for the partition of (if exists in any part) and insert into that partition. But if does not exist in either of the partitions, then we look for the partition of either or (either of these two must exist in or ) and insert into the other partition. -- To insert , we look for the partition of and insert into that partition. -- To insert , we look for the partition of (if exists in any part) and inset into that partition. But if does not exist in either of the partitions, then we look for the partition of either or and insert into the other partition. -- To insert , we look for the partition of and insert into that partition. • Step 4: When we insert a taxon to any part, we remove it from . After considering each and inserting taxa accordingly, if remains non-empty, we insert the remaining taxa to either part randomly. Obtaining , we search for a better partition iteratively. At each iteration, we perform a series of transfers of taxa from one partition set to the other to maximize the number of satisfied quartets. At the beginning of an iteration, we set the status of all the taxa as *free*. Then, for each *free* taxon , we calculate , and find the taxon with the maximum gain. There can be more than one taxa with the maximum gain where we need to break the tie. We will discuss this issue later. Next we transfer and set the status of this taxon as *locked* in the new partition that indicates that it will not be considered to be transferred again in this current iteration. This transfer creates the first intermediate bipartition . The algorithm then finds the next free taxon with the maximum gain with respect to , and transfer and lock that taxon to create another intermediate bipartition . Thus we transfer all the free taxon one by one. Let be the input quartet set and be the corresponding taxa set. Assume that  =  , , , , , (same as used in [Figure 4](#pone-0104008-g004){ref-type="fig"}). Hence, . Following the steps of the initial bipartition, we get the initial bipartition and . [Figure 5](#pone-0104008-g005){ref-type="fig"} shows the first iteration of the bipartition algorithm for this particular example. ![An example iteration of the Bipartition Algorithm MFM.\ The locked taxa are shown in circles. At each step, the taxon which has the maximum gain and will be transferred from its current partition to the other is indicated by a left arrow. (, ) is the initial bipartition of this iteration. Initially all taxa are free (i.e, not locked). The gain is computed for each free taxon of this step and the taxon (which is here) with maximum gain is transferred from its own partition to the other partition. Thus we get partition (, ), where is a locked taxon. In this way, only one taxon is locked at a step and once a taxon is locked, it remains locked throughout the iteration. An iteration completes when all taxa get locked. Here, all taxa get locked at (, ).](pone.0104008.g005){#pone-0104008-g005} Suppose that the taxa are locked in the following order: . That is, has been locked first, then , and so on. Let, the gain values of the corresponding partitions are: Now we define the cumulative gain up to the th transfer as The maximum cumulative gain, is defined as In each iteration, the algorithm finds the current ordering () of the transfers and saves this order in a log table along with the cumulative gains (see [Table 3](#pone-0104008-t003){ref-type="table"} for example). Let be the taxon in the log table corresponding to . This means that we obtain the maximum cumulative gain after moving the th taxon (with respect to the order stored in the log table). Then we rollback the transfers of the taxa () that were moved after . Let the resultant partition after these rollbacks is . This partition will be the initial partition for the next iteration. In this way, the algorithm continues as long as the maximum cumulative gain is greater than zero and returns the resultant bipartition. [Table 3](#pone-0104008-t003){ref-type="table"} lists the order of locking, corresponding gain and cumulative gain with respect to the iteration illustrated in [Figure 5](#pone-0104008-g005){ref-type="fig"}. From [Table 3](#pone-0104008-t003){ref-type="table"} we note that we get the maximum cumulative gain, , after moving taxon . Here, we also get the maximum value of cumulative gain after moving taxon . We break the tie arbitrarily. We consider the taxon for which we get the maximum cumulative gain for the first time. For this example, we get the maximum cumulative gain of at taxon for the first time. So we rollback all the subsequent moves. The resultant partition after this rollback is (partition in [Figure 5](#pone-0104008-g005){ref-type="fig"}). Similarly, [Table 4](#pone-0104008-t004){ref-type="table"} lists the ordering of locking, corresponding gain and cumulative gain with respect to the iteration which follows the iteration illustrated in [Figure 5](#pone-0104008-g005){ref-type="fig"}. From [Table 4](#pone-0104008-t004){ref-type="table"} we get that the maximum cumulative gain is . So the moves are rolled back and we get the final resultant partition . 10.1371/journal.pone.0104008.t003 ###### Gain Summary. ![](pone.0104008.t003){#pone-0104008-t003-3} -- -- -- -- -- -- -- -- The log table corresponding to the iteration shown in [Figure 5](#pone-0104008-g005){ref-type="fig"}. Here represents the step number. The input partition to step is (, ). The second column shows the taxon that has the maximum gain at the corresponding step, and the third column shows the corresponding maximum gain. The fourth column shows the cumulative gain of the gains listed in the third column. We observe that the cumulative gain gets maximum () after moving taxon in step . So all the subsequent moves of taxa are rolled back. The resultant partition of this iteration is (, )  =  , which is the initial partition for the next iteration of the iteration in [Figure 5](#pone-0104008-g005){ref-type="fig"}. 10.1371/journal.pone.0104008.t004 ###### Gain Summary. ![](pone.0104008.t004){#pone-0104008-t004-4} -- -- -- -- -- -- -- -- The log table corresponding to the next iteration of the iteration shown in [Figure 5](#pone-0104008-g005){ref-type="fig"}. Here represents the step number. The input partition to step is (, ). The second column shows the taxon that has the maximum gain at the corresponding step, and the third column shows the corresponding maximum gain. We observe that the cumulative gain gets maximum () at step . So we rollback all the subsequent moves including the move at step and return the initial partition of this iteration as the resultant bipartition of the bipartition algorithm. No more iteration is needed as the maximum cumulative gain of the current iteration is not greater than zero. As we have mentioned earlier, we do not allow any transfer of taxa that results into a singleton bipartition. Therefore, we need to add some additional conditions. Also, there could be more than one free taxa with the maximum gain, where we need to decide which one to transfer. We consider the following cases to address these issues. Let, be a set of free taxa with the maximum gain. • Case 1: and at least one corresponding bipartition is not singleton. That means, there exists such that transfer of does not result into a singleton bipartition. Let be the set of taxa, that can be safely transferred without resulting in a singleton bipartition. Note that, . If , we transfer the taxa . Otherwise, we have more than one taxa in . In that case, we pick the taxon , for which the corresponding bipartition (after transferring ) satisfies maximum number of quartets (note that every taxa in has the same gain, but the corresponding bipartitions do not necessarily satisfy the same number of quartets). In the case of a tie, we choose one taxon at random. • Case 2: and transfer of each results in a singleton bipartition. In this case, we consider the set of taxa with the second highest maximum gain. Let be the set of free taxa with the second highest maximum gain. We then recursively check 'Case 1' and 'Case 2' on . If we cannot find a taxon that can be transferred without resulting into a singleton bipartition, we make the status of all the free taxa *locked* and set their gain to zero. At each divide step we have a pair as input. The bipartition algorithm returns a bipartition of the taxa set . We then divide into and and obtain and pairs. and will be further bipartitioned in subsequent divide steps. The pseudo-code of the bipartition method MFM is given in Table S4 in [File S1](#pone.0104008.s001){ref-type="supplementary-material"}. Moreover, the run time analyses of Algorithm MFM is described in . Supporting Information {#s5} ====================== ###### **Supplementary material.** Additional tables, and the pseudocode and time complexity of MFM bipartition algorithm are presented. (PDF) ###### Click here for additional data file. We thank Dr. Sagi Snir for appreciating our work, providing constructive suggestions and helping us with the QMC code and data. [^1]: **Competing Interests:**The authors have declared that no competing interests exist. [^2]: Conceived and designed the experiments: RR MSB MSR. Performed the experiments: RR MSB. Analyzed the data: RR MSB MSR. Contributed reagents/materials/analysis tools: RR MSB. Wrote the paper: RR MSR MSB.
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Infection with *Mycobacterium tuberculosis* causes enormous worldwide morbidity and mortality; there were more cases of tuberculosis in 2007 (the last year for which data are available) than at any prior point in world history[@R1]. Among the factors that contribute to the continued growth of tuberculosis as a global health problem are the efficiency of human-to-human transmission by the aerosol route, the ability of the causal agent *M. tuberculosis* to persist and to progress despite development of host immune responses, and the absence of a vaccine with reliable efficacy in preventing transmission of the infection. Moreover, while attempts to control tuberculosis through improved identification and treatment of infectious cases have been successful in some settings, similar approaches in other contexts have resulted in increasing rates of resistance to available anti-tuberculosis drugs[@R2]. Therefore, new approaches to controlling tuberculosis are essential and would greatly benefit from an improved understanding of the biology of the bacteria and their interactions with their human hosts. In particular, understanding the factors that drive the evolution of *M. tuberculosis* and allow it to evade host defences, may suggest unique opportunities to develop novel strategies against tuberculosis. Human tuberculosis is caused by *Mycobacterium tuberculosis* and *Mycobacterium africanum*, which are members of the *M. tuberculosis* complex (MTBC). In addition to these human-adapted pathogens, MTBC includes various animal-adapted forms, such as *Mycobacterium bovis, Mycobacterium microti*, and *Mycobacterium pinnipedii*[@R3]. To characterize the extent and nature of the forces acting to diversify MTBC, we and others have applied several approaches to phylogenetic analysis of multiple clinical isolates from geographically diverse sources. Using single nucleotide polymorphisms (SNPs)^[@R3]-[@R6]^ or large sequence polymorphisms (LSPs)^[@R7]-[@R9]^ as genetic markers resulted in congruent groupings of human-adapted MTBC into six major lineages and consistent geographical associations for each of these lineages[@R10]. In addition, these studies found strong evidence for a clonal population structure of MTBC, without evidence of ongoing horizontal gene transfer. Analysis of SNPs in a total of 7 megabases of DNA sequence from 89 genes in 108 isolates of MTBC provided strong evidence that MTBC originated in Africa, and underwent population expansion and diversification following ancient human migrations out of Africa, followed by global spread and return to Africa of three particularly successful MTBC lineages through recent waves of travel, trade, and conquest[@R3]. Taken together, these studies have revealed that MTBC has undergone genetic diversification that corresponds to patterns of human migration, suggesting that distinct lineages have co-evolved with distinct human populations[@R7]. Moreover, they indicate that further understanding of the mechanisms and consequences of the interactions between MTBC and its human host can be obtained through comparative genomic analyses. Host-pathogen co-evolution is characterised by reciprocal adaptive changes in interacting species[@R11]. Host immune pressure and associated parasite immune evasion are key features of this process often referred to as an 'evolutionary arms-race'[@R12]-[@R13]. Studies in human pathogenic viruses, bacteria, and protozoa have revealed that genes encoding antigens tend to be highly variable as a consequence of diversifying selection to evade host immunity[@R14]-[@R17]. However, whether similar evolutionary mechanisms operate in MTBC, and whether the bacteria undergo antigenic variation in response to host immune pressure, is unknown. Immunity to tuberculosis in humans, nonhuman primates, and mice depends on T lymphocytes[@R18]. Among human T lymphocyte subsets, CD4^+^ T cells are clearly essential for protective immunity to MTBC, as demonstrated by the observation that the incidence of active tuberculosis in people infected with HIV is inversely proportional to the number of circulating CD4^+^ T cells[@R19]. In addition to CD4^+^ T cell responses, humans infected with MTBC develop antigen-specific CD8^+^ T cell responses[@R20], and MTBC antigen-specific human CD8^+^ T cells lyse infected cells and contribute to killing of intracellular MTBC[@R21]. Therefore, there is strong evidence that the adaptive immune system represented by CD4^+^ and CD8^+^ T cells, is an important mechanism for host recognition and control of MTBC. Recognition of foreign antigens by T lymphocytes depends on binding of short peptide fragments (termed epitopes) derived by proteolysis of foreign proteins, to MHC (major histocompatibility; in humans termed HLA (human leukocyte antigen)) proteins on the surface of macrophages and dendritic cells; CD4^+^ T cells recognize peptide epitopes bound to MHC/HLA class II; CD8^+^ T cells recognize peptide epitopes bound to MHC/HLA class I. To obtain a better understanding of the effects of human T cell recognition on the diversity of MTBC, and to test the hypothesis that MTBC uses antigenic variation as one mechanism of evading elimination by human immune responses, we determined the genome sequences of 21 phylogeographically diverse strains of MTBC and used those genome sequences to analyze the diversity of 491 experimentally verified human T cell epitopes. This analysis produced the unexpected finding that the known human T cell epitopes are highly conserved relative to the rest of the MTBC genome. These results provide evidence that the relationship between MTBC and its human hosts may differ from that of a classical evolutionary arms-race, and suggest that development of new approaches to control of tuberculosis must take into account the possibility that certain human immune responses may actually benefit MTBC. RESULTS {#S1} ======= A Genome-wide Phylogeny of Human-adapted MTBC {#S2} --------------------------------------------- A total of 22 mycobacterial strains were included in this work. To study the sequence diversity of T cell antigens in MTBC, we used Illumina next-generation DNA sequencing to generate nearly complete genome sequences from 20 strains representative of the six main human MTBC lineages, and one strain of *Mycobacterium canettii* which is the closest known outgroup of MTBC[@R3],[@R22] ([Table 1](#T1){ref-type="table"}). In addition, we used the published genome sequence of the H37Rv laboratory strain of *M. tuberculosis* as a common reference[@R23]. For each of the 21 strains newly sequenced, a mean of 6.8 million sequence reads with a mean length of 51 base pairs were generated and mapped to the H37Rv reference genome. On average, the reads covered 98.9% of the 4.4 Mb reference genome ([Table 1](#T1){ref-type="table"}). The regions not covered primarily included members of the highly GC-rich and repetitive PE/PPE gene families[@R24]. A total of 32,745 SNPs were identified, corresponding to an average of 1 SNP call for every 3 kb of sequence generated. We used a total of 9,037 unique SNPs (i.e. SNPs that occurred in one or several strains) to derive a genome-wide phylogeny of 22 strains ([Fig. 1](#F1){ref-type="fig"}**,**​ [Supplementary Fig. 1](#SD2){ref-type="supplementary-material"}). Six main lineages could be distinguished with high statistical support. These lineages were completely congruent to the strain groupings previously defined based on genomic deletion analysis and multilocus sequencing[@R3],[@R7],[@R10]. The perfect congruence between these different phylogenetic markers further corroborates the highly clonal population structure of MTBC and lack of ongoing horizontal gene transfer in this organism[@R25]. Because of the comprehensive nature of genome-scale data, a higher degree of phylogenetic resolution could be achieved compared to all previous studies. In this new phylogeny the brown and green lineages (also known as *Mycobacterium africanum*) are the most basal groups when compared to the *M. canettii* outgroup. *M. africanum* is highly restricted to West Africa for reasons that remain unclear[@R8]. However, the fact that the two *M. africanum* lineages represent the most ancestral forms of human MTBC reinforces the notion that human MTBC originated in Africa[@R3],[@R7]. Evolutionary Conservation Across Gene Categories {#S3} ------------------------------------------------ We used these genome sequence data and the phylogeny derived from them to compare the genetic diversity in antigens and other experimentally determined gene classes. For comparisons across different gene categories, we divided our dataset into three gene sets, including 'essential genes', 'non-essential genes', and 'antigens' ([Supplementary Fig. 2](#SD2){ref-type="supplementary-material"}**,**​ [Supplementary Tables 1 and 2](#SD2){ref-type="supplementary-material"}). Antigens were defined based on the presence of 491 experimentally confirmed human T cell epitopes ([Supplementary Table 3](#SD2){ref-type="supplementary-material"}), which were compiled through the Immune Epitope Database (IEDB) initiative[@R26]. The 'essential' gene category was defined based on genome-wide analyses of transposon insertion mutants that were defective for the ability to grow on Middlebrook 7H11 agar, or in the spleens of intravenously-infected mice, published previously[@R27]-[@R28]. We excluded from this analysis genes belonging to the PE/PPE gene family[@R24] and those related to mobile elements as they are difficult to study using current next-generation DNA sequencing technologies (total genes excluded: 273/3,990 (6.8%) genes annotated in the H37Rv reference genome; [Supplementary Table 4](#SD2){ref-type="supplementary-material"}). Based on evolutionary theory and findings in other bacteria[@R29], one would expect that in contrast to non-essential genes, the essential genes in MTBC will be under stronger purifying selection and thus more evolutionary conserved. In support of this notion, we observed that on average essential genes harboured less nucleotide diversity than non-essential genes ([Fig. 2](#F2){ref-type="fig"}; Mann-Whitney U test p\<0.002). We then compared the rates of synonymous and non-synonymous SNPs in the essential and non-essential gene categories. The synonymous and non-synonymous changes were derived by comparison to the most likely recent common ancestor of MTBC, which we inferred based on our new genome-wide phylogeny ([Fig. 1](#F1){ref-type="fig"}**,**​ [Supplementary Fig. 1](#SD2){ref-type="supplementary-material"}). Because MTBC harbours little sequence diversity, it was necessary to analyze the distribution of synonymous and non-synonymous SNPs based on gene concatenates rather than individual genes. The two measures of distribution we used were based on the number of non-redundant SNPs across all 21 MTBC strains (dN/dS based on Measure A in [Table 2](#T2){ref-type="table"} and [Fig. 3](#F3){ref-type="fig"}), and on the individual pairwise comparisons between each strain and the inferred most likely recent common ancestor (dN/dS based on Measures B in [Table 2](#T2){ref-type="table"}). From these analyses, we found that the dN/dS measures for essential genes were significantly lower than for non-essential genes (Measure A in [Fig. 3](#F3){ref-type="fig"}; Measure B in [Table 2](#T2){ref-type="table"}, Mann-Whitney U test p\<0.0001). Taken together, these data show that in MTBC essential genes are more evolutionary conserved than non-essential genes. Because MTBC interacts with humans through antigen-specific CD4^+^ or CD8^+^ T-cells, we would expect T cell antigens to be among the most diverse genes in the genome. Particularly when invoking a co-evolutionary arms-race and associated immune evasion, we would anticipate these antigens to be under diversifying selection and to be more variable than other genes in order to escape T cell recognition. However, when we analyzed the nucleotide diversity in 78 experimentally confirmed human T cell antigens ([Supplementary Table 2](#SD2){ref-type="supplementary-material"}), we found that they were on average not more diverse than essential genes ([Fig. 2](#F2){ref-type="fig"}, Mann-Whitney U test p=0.12). Moreover, we found that the dN/dS measures in these antigens also resembled those of essential genes (Measure A in [Fig. 3](#F3){ref-type="fig"}; Measure B in [Table 2](#T2){ref-type="table"}, Mann-Whitney U test p=0.77). Thus, human T cell antigens in MTBC do not appear to be under diversifying selection. Instead, purifying selection appears to be the driving selection pressure in these genes. T Cell Epitopes are Hyperconserved {#S4} ---------------------------------- T cell antigens consist of epitope regions that interact with human T cells, and non-epitope regions which are not targets of T cell recognition. Hence, we decided to study these regions separately. To this end, we generated a separate concatenate of the epitope regions and another concatenate of all corresponding non-epitope regions. Because little data is currently available in the IEDB with respect to whether these 491 epitopes are recognized by CD4^+^ or CD8^+^ T cells, we analyzed them as one class. If immune escape was driving antigen evolution to evade T cell recognition in MTBC, we would expect non-synonymous changes to accumulate in epitope regions, leading to a high dN/dS. Contrary to this expectation however, the overall dN/dS of the epitope regions was 0.53, which was still similar to essential genes and lower than non-essential genes ([Table 2](#T2){ref-type="table"}**,**​ [Fig. 3](#F3){ref-type="fig"}). Moreover, when we analyzed the distribution of amino acid replacements in individual epitopes we found that the large majority (95%) of the 491 epitopes showed no amino acid change ([Fig. 4](#F4){ref-type="fig"}). Only five epitopes, contained in *esxH, pstS1*, and Rv1986, harboured more than one variable position ([Supplementary Table 5](#SD2){ref-type="supplementary-material"}). The higher number of amino acid substitutions in these five epitopes may reflect ongoing immune evasion, but further investigation is needed to determine whether the observed changes are due to immune pressure, other selection pressure(s), or mere random genetic drift[@R3]. Because these five epitopes were clear outliers compared to the large majority of T cell epitopes analyzed here, we repeated our dN/dS analysis after excluding the three antigens harbouring the five outlier epitopes. Our analysis revealed that the epitope regions had the lowest dN/dS of all gene categories ([Table 2](#T2){ref-type="table"}, [Fig. 3](#F3){ref-type="fig"}). Furthermore, when we compared the proportion of non-redundant non-synonymous changes in epitope and non-epitope regions, we found that epitopes were less likely than non-epitopes to harbour changes at non-synonymous sites (Measure A in [Table 2](#T2){ref-type="table"}, χ^2^, p\<0.05), whereas no difference was observed at synonymous sites ([Table 2](#T2){ref-type="table"}, χ^2^, p=0.89). To further corroborate our finding of hyperconservation of human T cell epitopes in MTBC, we repeated our analysis using a data set from a previous study in which 89 individual genes were sequenced in 99 human-adapted strains representative of the six major global lineages of MTBC[@R3]. Sixteen of these 89 genes belonged to the T cell antigens analyzed here, including two of the three outlier antigens *esxH* and *pstS1*^[@R3]^. Analysis of this additional dataset of 16 antigens in 99 MTBC strains revealed an overall dN/dS for the epitope regions of 0.74. However, after excluding the two outlier antigens, the dN/dS dropped to 0.46, which was again lower than the genome-based dN/dS values for essential and non-essential genes ([Fig. 3](#F3){ref-type="fig"}). Taken together, our findings strongly suggest that a large proportion of the MTBC genome known to interact with human T cells is highly conserved and under as strong, or perhaps even stronger, purifying selection than essential genes. DISCUSSION {#S5} ========== In this study of 22 MTBC genomes, we demonstrate that, as expected, essential genes are more conserved than non-essential genes. These results are in agreement with a previous study which analyzed a single genome[@R30]. Surprisingly, however, we found that the large majority of the currently known T cell antigens are as conserved as essential genes. Furthermore, the epitope regions of these antigen genes are the most highly conserved regions we studied. This observation, that the regions of the genome that interact with the human adaptive immune system appear to be under even stronger purifying selection than essential genes, is inconsistent with a classical model of an evolutionary arms-race. It is possible that the known human T cell epitopes that we found to be hyperconserved represent a select subset of all of the human T cell epitopes encoded in the genome, and that certain approaches to epitope identification have favoured discovery of hyperconserved epitopes in MTBC. For example, since most, if not all of the epitope discovery efforts to date have utilized proteins and/or peptide sequences of strains from one lineage (lineage 4) and T cells from humans that are likely to have been infected by strains of other lineages, the assays used may have been especially suited to identification of hyperconserved and/or cross-reactive epitopes. While further investigation using alternative approaches to epitope discovery may reveal that variable epitopes that exhibit evidence of positive selection exist in the MTBC, it is likely that the large number of epitopes that we examined will remain a significant subset of the total, and that future vaccine development efforts will need to account for the possibility that immune recognition of certain epitopes may actually provide a net benefit to the bacteria. Lack of antigenic variation and immune evasion has been reported for a number of other human pathogens, including RNA viruses such as measles, mumps, rubella, and influenza type C[@R31]. Theoretical studies have suggested that the absence of immune escape variants in these viruses might be due to structural constraints in viral proteins or negative mutational effects leading to reduced infectivity or transmission[@R31]. While we cannot exclude the possibility that structural and functional constraints that are independent of T cell recognition contribute to hyperconservation of the regions encoding MTBC peptides recognized by human T cells, one important characteristic of the aformentioned viral pathogens is that they spread among young and immunologically naive hosts, which might eliminate the need for immune evasion[@R31]. Moreover, infection by these viruses usually results in acute disease, followed by elimination of the infection through adaptive immunity, and acquisition of lifelong immunity against re-infection. This further indicates that these viruses are specialized pathogens of immunologically naive hosts. By contrast, MTBC causes chronic and often lifelong infections, and adaptive immunity is usually unable to completely clear the infection[@R18]. Furthermore, tuberculosis patients are prone to re-infection[@R32], and mixed infections are also increasingly recognized[@R33]. These observations suggest that the biological basis for the lack of antigenic variation in MTBC reported here differs from what has been proposed for antigenically homogeneous RNA viruses[@R31]. In addition, we determined that the fraction of hyperconserved T cell epitopes of the MTBC that are derived from essential genes is indistinguishable from the frequency of essential genes in the MTBC genome as a whole (18% versus 21%, respectively; χ^2^ = 0.28, p = 0.59), indicating that our results were not skewed by over-representation of T cell epitopes in essential genes. Moreover, the T cell epitopes that we analyzed are present in genes from diverse gene ontologies, and the representation of five main gene categories (defined based on the NCBI Categories of Orthologous Groups (COG)) was no different in the T cell antigens when compared to the genome overall (χ^2^ with 4 degrees of freedom = 5.8, p = 0.21; [Supplementary Table 6](#SD2){ref-type="supplementary-material"}). Hence the only identifiable common property of these regions is their recognition by human T lymphocytes. These findings suggest that T lymphocyte recognition is an important factor in hyperconservation of these sequences, and that other structural or functional constraints are unlikely to fully account for the lack of sequence variation in these domains. Our data suggest that T cell epitopes in MTBC are under strong selection pressure to be maintained, perhaps because the immune response they elicit in humans, which are essential for survival of an individual host, might partially work towards the pathogen's benefit. One potential mechanism of benefit to MTBC from human T cell recognition is that human T cell responses are essential for MTBC to establish latent infection. This notion is supported by the fact that CD4^+^ T cell-deficient HIV-positive individuals progress rapidly to active disease after infection, rather than to sustain prolonged periods of latent tuberculosis[@R34]. Latent infection mediated by host T cell responses, with subsequent reactivation to active disease often occurring decades after initial infection, is a key characteristic of human tuberculosis, and might have evolved as a way for MTBC to transmit to later generations of susceptible hosts[@R35]. In addition, there is evidence that T cell responses may contribute directly to human-to-human transmission of MTBC. In particular, cavitary tuberculosis, which generates secondary cases more efficiently than other disease forms[@R36], rarely occurs in CD4^+^ T cell-deficient HIV-positive individuals, and the frequency of cavitary lung lesions in HIV-infected patients with tuberculosis is directly correlated with the number of peripheral CD4^+^ T cells[@R37]. While the mechanisms of lung cavitation in tuberculosis are poorly understood, these observations suggest that CD4^+^ T cells directly or indirectly mediate tissue damage in tuberculosis, and together with our finding of epitope hyperconservation indicate that certain T cell responses may be detrimental to the host and beneficial to the pathogen. Hence our findings suggest that MTBC takes advantage of host adaptive immunity to increase its likelihood of spread, and that the benefits of enhanced transmission exceed the costs of within-host cellular immune responses to these epitopes. In this manner, MTBC may resemble HIV, for which there is evidence that virulence has evolved, not to maximize replication of the virus within individual hosts, but to maximize the likelihood of its transmission[@R38]. Whether T cell responses to other epitopes, or whether specific T cell subsets (e.g. Th17 versus Th1) that benefit the host and not the bacteria can be identified will require additional studies in humans. One limitation of this study was the exclusion of PE/PPE genes because of technical reasons. Some of these genes are known to vary and to be cell-surface exposed, which has lead to the hypothesis they might be involved in antigenic variation[@R24]. However, no direct evidence for this has yet been presented. Future work will need to clarify the function and evolution of PE/PPE genes. By contrast, all the T cell antigens included in this study have been experimentally confirmed[@R26]. Furthermore, some of them are being targeted by new tuberculosis diagnostics and vaccines[@R39]. Our findings thus have important implications for the development of these new tools. On the one hand, the fact that MTBC harbours little sequence diversity in T cell antigens will facilitate the development of diagnostics that are universally applicable across geographical regions where MTBC strains differ[@R8]. On the other hand, the possibility that the immune responses induced by vaccine antigens might partially benefit the pathogen suggests current efforts in vaccine research should be broadened. Most disturbing is the suggestion that vaccine induced immunity against these conserved epitopes may perversely increase transmission. In this respect, it is interesting to note that the currently available tuberculosis vaccine Bacille-Calmette-Guerin (BCG), which is a live vaccine based on an attenuated from of *M. bovis*, offers no protection against pulmonary tuberculosis in adults[@R40]. More importantly, some clinical trials of BCG have even reported an increased risk of tuberculosis in vaccinees compared to unvaccinated individuals[@R41]. Thus, in contrast to standard reverse vaccinology, in which the least variable antigens of a genome are targeted[@R42], research into new tuberculosis vaccines should explore more variable regions of the MTBC genome. While most of the T cell epitopes anlyzed here were highly conserved, five epitopes in three antigens harboured a larger number of amino acid changes. The fact that the dN/dS measure dropped sharply after excluding these outlier antigens from the analysis further supports the notion that they are indeed outliers compared to the other antigens. One of these outlier antigens, *esxH* (Rv0288, also known as TB10.4) is a member of a gene family known to encode a Type VII secretion system[@R43]. Importantly, this antigen is being considered as new vaccine antigen against tuberculosis[@R39]. Thus even though most of the other vaccine antigens analyzed here are conserved, our finding that this particular vaccine antigen harbours a comparatively high number of amino acid substitutions across a panel of global MTBC isolates, suggests that strain diversity should be considered during further development of the new vaccine candidates containing *esxH[@R8]*. We detected significant differences in dN/dS between essential, non-essential, and antigenic genes. However, the individual dN/dS values remain high when compared to most other bacteria[@R44]. Such a high dN/dS was reported previously for MTBC, and has been linked to reduced selective constraint against slightly deleterious mutations[@R3]. It was proposed that the serial transmission bottlenecks associated with patient-to-patient transmission in MTBC could lead to an increase in random genetic drift compared to the forces of natural selection. Our new data show that even though the strength of purifying selection in MTBC might be reduced overall compared to other bacteria, it clearly is still acting on and capable of differentiating between gene categories. In summary, we show that T cell epitopes of MTBC are highly conserved, and do not reflect any ongoing evolutionary arms-race or immune-evasion. Instead, the patterns observed might be indicative of a distinct evolutionary strategy of immune-subversion developed by this highly successful pathogen. Other intracellular bacteria such as *Salmonella enterica* serovar Typhi exhibit a similar lack of antigenic variation[@R45], suggesting comparable mechanisms might exist in other pathogens with a similar lifestyle. Supplementary Material {#SM} ====================== We thank Fernando Gonzalez-Candelas, Sonia Borrell, and Douglas Young for comments on the manuscript. This project has been funded in whole or in part with Federal funds from the National Institute of Allergy and Infectious Disease, National Institutes of Health, Department of Health and Human Services, under Contract No. HHSN266200400001C. J.C. is a Howard Hughes Medical Institute Research Training Fellow. J.D.E. was supported by NIH grants AI046097 and AI051242, and S.G. by the Medical Research Council, UK, the Royal Society, the Swiss National Science Foundation, and NIH grants HHSN266200700022C and AI034238. METHODS Methods and any associated references are available in the online version of the paper at <http://www.nature.com/naturegenetics/>. **Accession codes.** The sequencing reads have been submitted to the NCBI Sequence Read Archive (SRA) with accession codes SRX002001-SRX002005, SRX002429, SRX003589, SRX003590, SRX005394, SRX007715, SRX007716, SRX007718-SRX007726, and SRX012272. Sequence and SNP data are also available at the Tuberculosis Database (TBDB). COMPETING INTEREST STATEMENT The authors declare no competing financial interests. ![Neighbour-joining phylogeny based on 9,037 variable common nucleotide positions across 21 human *M. tuberculosis* complex genome sequences. The tree is rooted with *M. canettii*, the closest known outgroup. Node support following 1,000 bootstrap replications is indicated. Branches are coloured according to the six main phylogeographic lineages of MTBC defined previously[@R3],[@R7]-[@R8]. Highly congruent topologies were obtained by Maximum likelihood and Bayesian inference ([Supplementary Fig. 1](#SD2){ref-type="supplementary-material"}).](ukmss-29888-f0001){#F1} ![Average gene-by-gene nucleotide diversity across three gene classes. Boxplot indicating median (horizontal line), interquartile range (box), and minimum and maximum values (whiskers).](ukmss-29888-f0002){#F2} ![Ratio of the rates of synonymous and non-synonymous substitutions (dN/dS) in various gene classes of MTBC. Overall dN/dS was calculated based on the number of non-redundant synonymous and non-synonymous changes after comparing each of the 21 MTBC genomes to the inferred most likely recent common ancestor of MTBC. This shows that essential genes are more conserved than non-essential genes, and that antigens are as conserved as essential genes. Figures for the epitope- and non-epitope regions refer to the calculations after excluding the three outlier antigens *esxH, pstS1*, and Rv1986.](ukmss-29888-f0003){#F3} ![Number of variable amino acid positions in 491 human T cell epitopes of MTBC. This demonstrates the remarkable lack of genetic variability among the regions of the genome that interact with the human immune system.](ukmss-29888-f0004){#F4} ###### Strains used in this study, sequencing coverage, and number of raw and filtered SNPs after comparison to the H37Rv reference genome ----------------------------------------------------------------------------------------------------------------------------------------------------------------------------- Strain Lineage[a](#TFN1){ref-type="table-fn"} Origin Average mapped\ Number\ Percent genome\ Raw SNPs Filtered SNPs sequencing depth of reads coverage[b](#TFN2){ref-type="table-fn"} -------------- ---------------------------------------- ----------------- ------------------ ----------- ----------------------------------------- ---------- --------------- MTB_95_0545 Lineage 1 Laos 77.37 7,621,946 99.75 3,478 2,017 MTB_K21 Lineage 1 Zimbabwe 77.99 7,112,888 99.29 2,853 2,151 MTB_K67 Lineage 1 Comoro Islands 78.29 7,097,284 98.95 2,943 2,070 MTB_K93 Lineage 1 Tanzania 65.52 6,017,391 99.22 2,949 2,041 MTB_T17 Lineage 1 The Philippines 72.59 7,130,412 99.36 3,788 1,988 MTB_T92 Lineage 1 The Philippines 46.01 5,068,053 98.85 4,080 1,994 MTB_00_1695 Lineage 2 Japan 77.92 7,394,236 99.02 2,875 1,351 MTB_98_1833 Lineage 2 China 64.49 6,395,114 99.1 2,962 1,361 MTB_M4100A Lineage 2 South Korea 40.47 4,022,290 98.94 3,316 1,354 MTB_T67 Lineage 2 China 78.77 7,616,603 98.73 2,820 1,343 MTB_T85 Lineage 2 China 61.65 6,159,284 99.04 3,046 1,377 MTB_91_0079 Lineage 3 Ethiopia 74.03 7,228,038 99.14 2,920 1,363 MTB_K49 Lineage 3 Tanzania 75.52 6,845,266 99.25 2,195 1,416 H37Rv Lineage 4 USA Reference MTB_4783_04 Lineage 4 Sierra-Leone 78.12 7,466,814 98.78 1,559 741 MTB_GM_1503 Lineage 4 The Gambia 82.26 7,891,933 99.08 2,283 782 MTB_K37 Lineage 4 Uganda 59.86 5,480,451 98.85 2,496 822 MAF_11821_03 Lineage 5 Sierra-Leone 78.22 7,491,737 99.02 3,741 2,102 MAF_5444_04 Lineage 5 Ghana 79.75 7,578,690 98.92 3,686 2,079 MAF_4141_04 Lineage 6 Sierra-Leone 72.62 7,027,143 98.61 3,886 2,180 MAF_GM_0981 Lineage 6 The Gambia 76.39 7,350,873 99 4,451 2,213 MTB_K116 *M. canettii* Somalia 93.01 6,544,254 96.32 19,008 14,730 Total MTBC 62,327 32,745 ----------------------------------------------------------------------------------------------------------------------------------------------------------------------------- **Notes:** Defined as in [@R8]. Compared to the reference genome H37Rv. ###### Distribution of synonymous and non-synonymous SNPs in gene concatenates -------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- Gene category Length of\ Measure A[a](#TFN3){ref-type="table-fn"} Measure B[b](#TFN4){ref-type="table-fn"} Concatenate\ (base pairs) -------------------------------------------------- -------------- ------------------------------------------ ------------------------------------------ ------ ----------------------------------- ----------- **Essential** 907,584 1,124.83 755.17 1.49 0.53 0.45-0.67 **Non-essential** 2,674,329 4,392.51 2,338.49 1.88 0.65 0.78-0.56 **Antigens** 81,660 126.5 87.5 1.45 0.57 0.17-1.15 **Epitopes** 12,234 19 12 1.58 na[d](#TFN6){ref-type="table-fn"} na **Epitopes** [c](#TFN5){ref-type="table-fn"} 11,088 9 12 0.75 na na **Non-epitopes** [c](#TFN5){ref-type="table-fn"} 68,556 106.5 75.5 1.41 na na -------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- **Notes:** The number of non-redundant synonymous and non-synonymous SNPs after mapping the changes onto the phylogeny shown in [Figure 1](#F1){ref-type="fig"}. An overall dN/dS was calculated based on these SNPs and is shown in [Figure 3](#F3){ref-type="fig"} (Measure A; see Materials and Methods). Calculated using Measure B. The median dN/dS was calculated from the 21 strain specific dN/dS values. This measure of dN/dS could only be calculated for the essential, non-essential and antigen categories because in the epitope and non-epitope concatenates some strains had zero values for synonymous or non-synonymous changes. After exclusion of the three outlier antigens *esxH, pstS1*, and Rv1986 (see main text). not applicable. [^1]: AUTHOR CONTRIBUTION STATEMENTS I.C., J.D.E. and S.G. designed the study; P.M.S., S.N., K.K. and S.G. contributed sources of *M. tuberculosis* DNA and demographic information; I.C., J.C. and J.G. performed DNA sequencing and bioinformatics; I.C., P.M.S., J.D.E. and S.G. wrote the manuscript with comments from all authors.
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The execution steps in most research, development, and engineering experiments generally involve manual operations carried out on unconnected technology platforms. The scientist or engineer works in what are essentially isolated technology islands with manual operations providing the only bridges. To illustrate, when there is a Standard Operating Practice (SOP) Guide for the experimental work, it is often an electronic document, for example in Microsoft Word. The experimental plan (Step 1) within the SOP Guide has to be transferred to the target device (instrument, instrument platform, or component module for execution (Step 2) by manually re-keying the experiment into the device's instrument control program (ICP)—the device's controlling application software. In a few cases the statistical analysis of results (Step 3a) can be done within the ICP, but it is most often done within a separate statistical analysis software package or spreadsheet program such as Microsoft Excel. This also requires manually transferring the results data from the ICP to the analysis software package. Reporting of results (Step 3b) is usually carried out in Microsoft Word, and therefore requires the manual transfer of all results tables and graphs from the separate statistical analysis software package. The manual operations within the general execution sequence steps are presented below. The isolated technology islands are illustrated in FIGS. 1 and 2. FIG. 1 illustrates the manual tools and operations involved in carrying out a research and development experiment. In this work a statistical experiment design protocol is first generated, via step 12. This protocol is developed manually and off-line using non-validated tools such as Microsoft Word. The protocol then must be approved, once again manually and off-line, via step 14. When required, sample amounts are then calculated using non-validated tools such as Microsoft Excel, via step 16. Thereafter the samples are prepared, via step 18 and the experiment is run on a target device, via step 20, for example, a high-performance liquid chromatograph (HPLC). Running the experiment requires manually re-constructing the statistical design within the target device's ICP. When this software does not exist, or does not allow for full instrument control, the experiment must be carried out in a fully manual mode by manually adjusting instrument settings between experiment runs. FIG. 2 illustrates the manual tools and operations involved in analyzing the data and reporting the results of the research and development experiment, via step 22. The analysis and reporting of data is accomplished by first statistically analyzing and interpreting the experiment data, off-line, using non-validated tools such as Microsoft Excel. Next, it is determined whether or not there is a need for more experiments, possibly using off-line generic Design of Experiments (DOE) software, via step 24. Then, data are entered and a report is written, via step 26. Finally, the report is archived, via step 28. As is seen from the above, the research, development, and engineering experimentation process involves a series of activities that are currently conducted in separate “technology islands” that require manual data exchanges among the tools that are used for each activity. However, until now, no overarching automation technology exists that brings together all the individual activities under a single integrated-technology platform that is adapted to multiple devices and data systems. Method development activities encompass the planning and experimental work involved in developing and optimizing an analytical method for its intended use. These activities are often captured in company Standard Operating Procedure (SOP) documents that may incorporate Food and Drug Administration (FDA) and International Conference on Harmonization (ICH) requirements and guidances. Method development SOP documents include a description of all aspects of the method development work for each experiment type (e.g. early phase analytical column screening, late phase method optimization, method robustness) within a framework of three general execution sequence steps: (1) experimental plan, (2) instrumental procedures, and (3) analysis and reporting of results. The individual elements within these three general steps are presented below. Step 1: Generate Experimental Plan Select experiment type Select target instrument Define study variables: analyte concentrations instrument parameters environmental parameters Specify number of levels per variable Specify number of preparation replicates per sample Specify number of injections per preparation replicate Integrate standards Include system suitability injections Define Acceptance Criteria Step 2: Construct Instrumental Procedures Define required transformations of the experiment plan into the native file or data formats of the instrument's controlling ICP software (construction of Sample Sets and Method Sets or Sequence and Method files). Specify number of injections (rows) Specify type of each injection (e.g., sample, standard) Step 3: Analyze Data and Report Results Specify analysis calculations and report content and format Carry out numerical analyses Compare analysis results to acceptance criteria (FDA & ICH requirements) Specify graphs and plots that should accompany the analysis Construct graphs and plots Compile final report The execution steps in analytical method development generally involve manual operations carried out on unconnected technology platforms. To illustrate, an SOP Guide for the development of an HPLC analytical method is often an electronic document in Microsoft Word. The experimental plan (Step 1) within the SOP Guide has to be transferred to the HPLC instrument for execution (Step 2) by manually re-keying the experiment into the instrument platform's ICP—in the case of an HPLC this is typically referred to as a chromatography data system (CDS). In a few cases the statistical analysis of results (Step 3) can be performed within the CDS, but it is most often carried out within a separate statistical analysis software package or spreadsheet program such as Microsoft Excel. This also requires manually transferring the results data from the CDS to the analysis software package. Reporting of results (Step 3) is usually carried out in Microsoft Word, and therefore requires the manual transfer of all results tables and graphs from the separate statistical analysis software package. The manual operations within the three general execution sequence steps are presented below. Step 1—Experimental Plan Development plan developed in Microsoft Word. Experimental design protocol developed in off-line DOE software. Step 2—Instrumental Procedures Manually build the Sequences or Sample Sets and instrument methods in the CDS. Raw peak (x, y) data reduction calculations performed by the CDS (e.g. peak area, resolution, retention time, concentration). Step 3a—Statistical Analysis Calculated results manually transferred from the CDS to Microsoft Excel. Statistical analysis usually carried out manually in Microsoft Excel. Some graphs generated manually in Microsoft Excel, some obtained from the CDS. Step 3b—Reporting of Results Reports manually constructed from template documents in Microsoft Word. Graphs and plots manually integrated into report document. It is realized that prior art systems in the area do not address the overarching problem of removing the manually intensive steps required to bridge the separate technology islands. Similarly, it is also realized from the prior art that inherent data loss is known to occur in sampling of experimental results to impact quantitative effect estimations and thereby degrade and typically render inaccurate statistical confidences from experimental results. However, the prior art is not instructive in assisting in overcoming these problems to improve the accuracy or analyzability of experimental results and sampling, nor is the prior art instructing in overcoming deficiencies enabling one to develop a readily obtainable solution to overcome inherent data loss, provide an identifiable metric for separate experimental undertakings, or provide information about resulting effects where experimental samples contain inherent data losses. For instance, often trial runs of research and development (R&D) experiments may be carried out by making changes to one or more controllable parameters (as used herein such may include but not be limited to study factors, instrument settings, controllable parameters of instrumentation, a set of discrete process events, or other experimentation factors with other factors remaining constant (as used herein the controlled portion of an experiment or experimental run or trial) of a process or system and then measuring test samples obtained from in-process sampling or process output. Typically, an objective of a researcher in these undertakings is to identify and quantify the effects of the parameter changes on the identified important process output quality attributes or performance characteristics that are being measured. The quantified effects can then be used to define the parameter settings that will give the desired process output results. FIG. 3 illustrates a generalized flow diagram of a process in a predetermined process flow direction (305) consisting of four discrete elements (300): base material input (310), key reactant input (320), heating (330), and chemical reaction (340). For the avoidance of doubt, FIG. 3 and its related embodiments are foundational to the present invention herein. The flow diagram 300 also contains an in-process measurement step at 335 and a process endpoint measurement step at 350. In this generalized process 300 the base material element may have one or more controllable parameters such as material feed rate or be of two or more blended components including base material formulation for example. In addition, the measurements of the quality attributes or performance characteristics of interest may actually be taken within the process stream, as would be done by an in-process measurement system, or on the process output material. The process 300 of FIG. 3 can similarly be analogized via a chemical separation process performed by instrumentation such as that of an HPLC. FIG. 4A is demonstrative of such an adaptation of the general process flow diagram 300 of FIG. 3 to that of an HPLC. In FIG. 4A, the flow diagram 400 comprises three primary HPLC process elements: solvent delivery (410), sample injection (420), and a separation chamber (430). In FIG. 4A, method development experiments may be performed on controllable parameters within the HPLC to identify the parameter settings that are optimum for the separation of a given mixture of compounds. In such experiments, one critical performance characteristic being measured, for example, may be the degree of separation of the mixture into isolated pure individual compounds, as is further defined by the legend at 440. However, and more particularly in typical practical applications such as those within the pharmaceutical industry, the active pharmaceutical ingredient (API) and one or more degradants and/or impurities in a drug product often represents a normal mixture of compounds for which an HPLC method must be developed. As is known from practical applications under tradition methods, accurately measuring the amount of API in a test sample (or actual sample) with an HPLC would require that the instrument first separate the API from the degradants and/or impurities. As used herein, the term “impurities” are defined to include but not be limited to components of the drug product formulation, which may also be termed excipients, or contaminants that come from various points or stages in the process or even the product packaging of an affected product or sample. For example, an impurity may be a plastic compound from a product container that may contaminate the surface of the drug tablet for instance. By further example, a test sample may be a dissolved tablet (i.e., the solid dosage form of the drug product) that contains the API and impurities. As used herein, the term “degradants” are defined as breakdown products of a sample API or impurity, i.e., molecules which result from the decomposition of the API or impurity. As an additional further example, a test sample may be a dissolved tablet (i.e., the solid dosage form of the drug product) that is subject to stress conditions which attempt to force the degradation of the API and impurity compounds in the sample. Therefore a critical HPLC method development experiment objective in a traditional practice application may include identifying the instrument operating conditions that separate the API from any degradants and impurities in a test mixture to the degree required (i.e., accuracy level) to accurately measure the API amount. Further in separation method development experiments, for example, some of the HPLC parameter settings used in the experiment trials can result in the inability to accurately measure a critical performance characteristic, such as compound separation. These issues are known to be a significant challenge for researchers and commercial entities alike. The consequences of these limitations realized by many in the field then are the inherent data losses in one or more experiment trials which can then result in the inability to quantitatively analyze the experiment results and draw any meaningful conclusions. FIG. 4B depicts an instrument hardware framework 450 associated with an HPLC instrument system. The HPLC framework 450 comprises several process elements with controllable parameters that can be experimentally addressed. The process elements include: solvent formulation and solvent pH adjusted using a controllable valve module for solvent selection (CVM—Solvent Switching) (451), the solvent flow rate (Pump Module) (452), the type of separation column adjusted using a controllable valve module for column switching (CVM—Column Switching) (453), a sampler (454) and a detector (455). For FIG. 4B, a typical experiment (i.e., method development experiment) may be comprised of conducting one or more trials where a trial consists of operating the HPLC instrument at one or more predetermined settings of the study parameters, injecting a small amount of the sample mixture into the solvent stream and measuring critical performance characteristics such as the degree of separation of the individual sample compounds at the endpoint of the process 455. By exemplar, objectives of experimentation under the framework of FIG. 4B in view of the process set forth in FIG. 4A, may include attempting to separate out one or more APIs from impurities or degradants. In such experiments, for example, the controllable parameters of the CVM modules (451 and 453) and the Pump Module (452) may be selected for experimental study. In such experiments, CVM solvent switching parameters may be adjusted between experiment trials to deliver a solvent mix at a different pH and the results captured. In such experiments, CVM column switching parameters may also be adjusted so as to employ a different column, for example, in each experimental trial undertaken. Similarly, in such experiments, pump module parameters may be adjusted between trials to both change the rate at which the solvent formulation is changed (i.e., proportion of organic solvent increased) during a trial run and to deliver the solvent formulation at a different flow rate. However, as will become further evident, in these types of experiments, despite the objectives of experimentation including attempts to separate out one or more APIs from impurities and/or degradants by selecting predetermined controllable parameters for experimental study, the results can be inaccurate. FIG. 4C depicts a graphical chromatogram representation 460 of experimental results data obtained from a particular trial run trial in one of the experimental runs under assessment herein (e.g. trial run 11), wherein the “raw” results depicted in the figure are in the form of “absorbance peaks.” A peak typically occurs when a compound absorbs light transmitted through the solvent stream and is detected by the detector as the compound passes the detector at a given time X, wherein the baseline condition represents zero absorbance of the light. As used herein, an “absorbance peak” or “peak” generally means a vertical spike (Y axis deviation) along a horizontal line in the graph from baseline conditions (where Y=zero) occurring at a given X axis time interval. As also used herein, a compound's “retention time” is defined as the time from injection to detection, and, in the chromatogram, this time is the X-axis value corresponding to the peak's maximum Y value. In FIG. 4C, poorly separated peaks are apparent at 461 and 462. Interpretatively, each peak in FIG. 4C corresponds to at least one compound (i.e., the API or an impurity). It should also be readily recognized that the area under a given peak is proportional to the amount of absorbed light, which is in turn proportional to the amount of the corresponding compound in the solvent stream passing the detector at the time indicated on the X axis in the chromatogram. However, problematically, translating the measured area of a given peak into an amount of the corresponding compound is typically accurate only where the peak in a chromatogram is the result of only one compound. As a result, accurately measuring the amount of an individual compound in a sample using traditional approaches is difficult and often impossible when two or more compounds pass through the detector at the same time due to lack of separation (i.e., 461 and 462). Unfortunately, the occurrence of two or more compounds passing through the detector at the same time due to lack of separation is quite a common event in many method development experiment instances. To attempt to compensate for this limitation, often a primary goal of many HPLC method development experiments is to identify the instrument settings that result in a chromatogram with the following critical characteristics: (1) an observable peak being present for each compound in the sample, (2) situations where each peak is separated from all other peaks (i.e., no overlap) to a degree at least minimally necessary to accurately quantify the amount of the corresponding compound in the sample, and (3) the separation of a critical peak, often an API, from its nearest peak. The degree of separation between a given pair of adjacent compound peaks in a chromatogram is defined herein as the “peak resolution.” In a traditional approach to HPLC method development, the effect of instrument setting changes on the resolution of sample compounds is therefore typically relied on as being one of the most important experiment results. As a result, it is traditionally believed and practiced to carry out the following steps: a. change one or more instrument settings, inject a sample, and obtain a resulting chromatogram; b. associate each peak in the chromatogram with one of the sample compounds; c. compute the peak resolution results for all adjacent peak (compound) pairs; d. determine if the compounds are sufficiently separated, as represented by the adjacent peak pair resolution data, to accurately determine the amount of each compound in the sample to the required level of precision; and e. repeat Steps (a)-(d) above if the compounds are not sufficiently resolved. Unfortunately, the correct assignment of the sample compounds to the chromatogram peaks as in Step (b) above is critical to accurately interpret experiment trial results in accordance with traditional practice. Such traditional practice characteristics may include current numerical analysis approaches and the like. Since, as is often the situation, current analysis and interpretation approaches target the interactions of each compound with the HPLC system elements that result from the specific chemical and structural nature of the compound, determining specifically and precisely which compound each resolution result associates with, in a given chromatogram, is effectively the only way to track the effects of instrument changes on the separation of that compound. A further complication especially common to early HPLC method development experiments that involve analytical column and pH screening has been that it may not be readily determinable as to how many compounds are in an experimental sample, and therefore how many peaks an experimenter is to expect in a chromatogram obtained from sample analysis by HPLC. This particular complication is further illustrated by comparing FIG. 4C with FIG. 4D. FIG. 4D is a chromatogram 470 obtained from the same sample of FIG. 4C as analyzed under different trial settings of the HPLC instrument. The chromatogram of FIG. 4D shows twelve well separated peaks being visible along the X axis time interval of 10 to 34 minutes (see for example representative peaks at 471 and 472, where an uncertain or undefinable number of peaks exist in this same interval in FIG. 4C (see for example representative points at 461 and 462). However, additional complications can result even where the number and identity of all compounds in a test sample are known as such knowledge does not necessarily simplify the work of correctly associating each peak with a sample compound in each trial chromatogram, since instrument changes between trials can affect both peak shape (i.e., broad-flat versus narrow-spiked) and the column transit time of the corresponding compound (i.e., peak retention time). For example, for a particular experimental trial, a peak arising in a resulting chromatogram corresponding to a given compound may occur at 15 minutes and appear narrow and spiked. In a second trial with different instrument settings, the peak corresponding to the same compound may occur at 12 minutes and may appear as being broad and flat. Contradistinctively, a third trial's settings may cause a second peak to also occur at the 12 minute location in the chromatogram resulting in a combined peak that differs greatly in shape and area from the others. By further example, in FIG. 4C at 461, overlapping peaks corresponding to incompletely separated compounds can be seen, and again at 462, while peaks with the same or very similar shape and area in FIG. 4D occur at approximately 22, 23, and 24 minutes (473, 474, and 475 respectively).
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The Village of New Gourna The Village of New Gourna by Lara Iskander Famous architect and artist, Hassan Fathy was born in Alexandria in 1899 to an Egyptian father and a Turkish mother. He studied at Cairo University and later became a professor at the Faculty of Fine Arts and was head of the Architectural School. He was an architect who devoted himself to housing the poor in developing nations. He aimed to create affordable and livable spaces suitable to the surrounding environment, thus improving the economy and the standard of living in rural areas. Nevertheless, Hassan Fathy was not very successful at convincing the state of his ideas. His work was considered to be ahead of his time as they were not always welcomed by the government bureaucrats neither were they to the tastes of poor Egyptians peasants who longed for the "luxury" of the concrete city buildings. Fathy's buildings were distressingly inexpensive. This was seen as a back draw. Hassan Fathy was strongly against Western techniques and materials like reinforced concrete and steel which he found inappropriate for Egypt's climate and the craftsmen's limited skills. "Matchbox houses" were too hot in the summer and too cold in winter. He encouraged ancient design methods and materials. He saw a more appropriate method of building in the Vernacular Architecture of the Nubians (region of southern Egypt), which influenced his ideas greatly. Nubian craftsmen were masters at constructing domed and vaulted roofs of mud brick which they also used for the walls. The structures were cheap, cool in the summer and the walls were heat-retaining in winter. While implementing the Nubian building techniques, he aimed to train Egyptian craftsmen to build their houses using mud brick or Adobe, which was ideally suitable to the local conditions of Upper Egypt and at a fraction of the cost. New Gourna Project is one of his best known housing projects. This is due to the international popularity of his book, "Architecture for the poor" published originally in French, 20 years after the beginning of the project, in which he explained his vision for the village. This book details his thoughts, processes, dealings with the politics involved, and his theories behind the forms. The idea was launched by the Egyptian department of Antiquities in 1946 to build a new town near Luxor to relocate the inhabitants of the Gourna Village or also called "Sheikh Abd el-Qurna". The old Gourna village is built over Pharaonic tombs, many of which were not discovered yet. The residents were famous for being able to bring up suspiciously authentic Egyptian monuments from their cellars. The antiquities were having trouble controlling the tomb-robbing occurring in the areas of the Valley of the Kings, Queens and Nobles nearby. And so, the perfect solution seemed to be to move the seven thousand locals whose economy depended on tomb looting. This came as Fathy's perfect opportunity. The new location is about five miles downhill towards the river, not far from the old village. Hassan Fathy's saw this as a challenge, as he says in his book. Faced with a 50 acre land intended to home 7000 people unwilling to leave their homes was not to be an easy task. His designs depended on natural ventilation, orientation and local materials, traditional construction methods and energy- conservation techniques. He carried out detailed studies of temperature and wind patterns. Hassan Fathy did not believe that the locals should be housed in similar homes. Each had different needs, tastes and comforts apart from the number living in the house. Fathy worked with the villagers to tailor his designs to their needs with creativity and variety keeping the same spirit to the entire village. Fathy included an open air theatre, a school, a "Suq" (market) and a Mosque, famous for the unusual shape of its minaret. He also built himself a house in the same spirit of the village, using the same materials. The "Gourna Village experiment" was not just an architectural experiment. To Hassan Fathy it was more like the development of a town on a cultural, social level following the regional traditions. Relating to the people and knowing their needs while asking them to participate in the construction of their town was a major part of the project. The village was never completed. The locals did start moving into their new homes, but eventually they did not settle down. The reluctance of the people to cooperate in the design and building of the village was mistakenly understood as a sure sign of the inappropriateness the project. Normally, the people resented the change and took every opportunity possible to sabotage their new village in order to stay where they were and to continue their own secret ancient trading. It did not take long to see the beginning of the failure the village. The village was never completed. All what remains today of New Gourna is the mosque, market, a couple of houses and Hassan Fathy's. Even the school was demolished and rebuilt in modern materials. As for the rest of the houses, most of them were rebuilt in a more "suitable" way according to the people's taste. In 1967, he had another trial similar to Gourna called the village of Bariz in Kharga. It didn't not prove to be a better success from the previous because of funding problems. His numerous honors include the International Gold Medal Award from the International Union of Architects and the Aga Khan award he received in 1980. Hassan Fathy's ideas are now more in vogue. Though not exactly his aim, his style of structures has become very famous between the upper classes that tend to use the traditional vaults and domes for roofing. Also, many touristic resorts such as El Gouna near Hurghada have followed this theme. It was partially built by one of his students and is obviously a great success. The remains of these villages are worth a visit. His buildings have proven to be very efficient, comfortable, spacious, always based on natural resources and most convenient to hot climate. Fathy designed several projects abroad in such places as New Mexico and India. His files, drawing and notes are all kept at the AUC rare collections where they are exhibited. Resource: Original research by Lara Iskander Last Updated: June 9th, 2011 Who are we? Tour Egypt aims to offer the ultimate Egyptian adventure and intimate knowledge about the country. We offer this unique experience in two ways, the first one is by organizing a tour and coming to Egypt for a visit, whether alone or in a group, and living it firsthand. The second way to experience Egypt is from the comfort of your own home: online.
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Used rubber tires have been causing a pollution problem since they replaced the wagon wheel. They are bulky, do not break down on their own, and quickly cause landfills to fill up. On occasion, used tires catch fire and can burn for days or weeks, releasing harmful pollutants both into the atmosphere and into the groundwater. Some efforts have been made to chop up used tires and reassemble them into a useful product. With glue or heat, chopped tires can be made into floor padding for gyms, machine shops and playgrounds. Chopped tires can be used as mulch or ground cover or they can be used to manufacture sandals, welcome mats and rubber speed bumps. The problem of removing steel belts from tires is difficult to solve, so tires with steel belts may not be suitable for recycling in these applications. Another problem is that making these products from recycled tires costs more than making them from virgin materials, and customers are suspicious that the recycled products may contain carcinogens and other hazardous substances. Therefore, the cost of recycling used tires and public suspicion of them remain issues to be resolved. Another option for recycling used tires is heat-based pyrolysis. For example, U.S. Pat. No. 8,475,726 for “Reactor and apparatus for pyrolyzing waste, especially tyres” discloses heating used tires to cause them to pyrolize, allowing separation of oils, metal and carbon black. Decades of experimentation with such systems have shown them to be energy-inefficient, resulting in most used tires making their way to landfills. Such systems also have a problem with leaving hazardous materials, including heavy metals, in the recycled material. An alternative method for recycling used tires is to break down the vulcanized chemical bonds through radio frequency pyrolysis. Such systems in theory hold academic promise but have not proven commercially viable. Another method for recycling tires employs chemical devulcanization through the addition of diphenyl disulfide and heat to the tires. This system has proven to be dirty, expensive to implement, and creates a substantial pollution problem. Photo devulcanization processing of used tires is another possibility. In this system, the recycler mixes a photoreactive material with used tires and exposes the photoreactive material to light. The light causes the photoreactive material to build up heat and pyrolize the tire. This method has not been commercially successful due to the problem of chopped used tires being opaque. Therefore there is a need for a method for recycling used tires which is energy-efficient, does not cause environmental pollution, and deals with the issues of steel in the tires as well as hazardous waste that tire recycling can create.
3.28125
3
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Display devices for use in TVs, cell phones, etc., and optical elements, such as camera lenses, etc., usually adopt an antireflection technique in order to reduce the surface reflection and increase the amount of light transmitted therethrough. This is because, when light is transmitted through the interface between media of different refractive indices, e.g., when light is incident on the interface between air and glass, the amount of transmitted light decreases due to, for example, Fresnel reflection, thus deteriorating the visibility. An antireflection technique which has been receiving attention in recent years is forming over a substrate surface a very small uneven pattern in which the interval of recessed portions or raised portions is not more than the wavelength of visible light (λ=380 nm to 780 nm). See Patent Documents 1 to 4. The two-dimensional size of a raised portion of an uneven pattern which performs an antireflection function is not less than 10 nm and less than 500 nm. This method utilizes the principles of a so-called moth-eye structure. The refractive index for light that is incident on the substrate is continuously changed along the depth direction of the recessed portions or raised portions, from the refractive index of a medium on which the light is incident to the refractive index of the substrate, whereby reflection of a wavelength band that is subject to antireflection is prevented. The moth-eye structure is advantageous in that it is capable of performing an antireflection function with small incident angle dependence over a wide wavelength band, as well as that it is applicable to a number of materials, and that an uneven pattern can be directly formed in a substrate. As such, a high-performance antireflection film (or antireflection surface) can be provided at a low cost. As the method of forming a moth-eye structure, using an anodized porous alumina layer which is obtained by means of anodization of aluminum has been receiving attention (Patent Documents 2 to 4). Now, the anodized porous alumina layer which is obtained by means of anodization of aluminum is briefly described. Conventionally, a method of forming a porous structure by means of anodization has been receiving attention as a simple method for making nanometer-scale micropores (very small recessed portions) in the shape of a circular column in a regular arrangement. An aluminum base is immersed in an acidic electrolytic solution of sulfuric acid, oxalic acid, phosphoric acid, or the like, or an alkaline electrolytic solution, and this is used as an anode in application of a voltage, which causes oxidation and dissolution. The oxidation and the dissolution concurrently advance over a surface of the aluminum base to form an oxide film which has micropores over its surface. The micropores, which are in the shape of a circular column, are oriented vertical to the oxide film and exhibit a self-organized regularity under certain conditions (voltage, electrolyte type, temperature, etc.). Thus, this anodized porous alumina layer is expected to be applied to a wide variety of functional materials. A porous alumina layer formed under specific conditions includes cells in the shape of a generally regular hexagon which are in a closest packed two-dimensional arrangement when seen in a direction perpendicular to the film surface. Each of the cells has a micropore at its center. The arrangement of the micropores is periodic. The cells are formed as a result of local dissolution and growth of a coating. The dissolution and growth of the coating concurrently advance at the bottom of the micropores which is referred to as a barrier layer. As known, the interval between adjacent micropores (the distance between the centers), is approximately twice the thickness of the barrier layer, and is approximately proportional to the voltage that is applied during the anodization. It is also known that the diameter of the micropores depends on the type, concentration, temperature, etc., of the electrolytic solution but is, usually, about ⅓ of the size of the cells (the length of the longest diagonal of the cell when seen in a direction vertical to the film surface). Such micropores of the porous alumina may constitute an arrangement which has a high regularity (periodicity) under specific conditions, an arrangement with a regularity degraded to some extent depending on the conditions, or an irregular (non-periodic) arrangement. Patent Document 2 discloses a method of producing an antireflection film (antireflection surface) with the use of a stamper which has an anodized porous alumina film over its surface. Patent Document 3 discloses the technique of forming tapered recesses with continuously changing pore diameters by repeating anodization of aluminum and a pore diameter increasing process. The applicant of the present application discloses, in Patent Document 4, the technique of forming an antireflection film with the use of an alumina layer in which very small recessed portions have stepped lateral surfaces. As described in Patent Documents 1, 2, and 4, by providing an uneven structure (macro structure) which is greater than a moth-eye structure (micro structure) in addition to the moth-eye structure, the antireflection film (antireflection surface) can be provided with an antiglare function. The two-dimensional size of a raised portion of the uneven structure which is capable of performing the antiglare function is not less than 1 μm and less than 100 μm. Utilizing an anodized porous aluminum film can facilitate the manufacture of a mold which is used for formation of a moth-eye structure over a surface (hereinafter, “moth-eye mold”). In particular, as described in Patent Documents 2 and 4, when the surface of the anodized aluminum film as formed is used as a mold without any modification, a large effect of reducing the manufacturing cost is achieved. The structure of the surface of a moth-eye mold which is capable of forming a moth-eye structure is herein referred to as “inverted moth-eye structure”. A known antireflection film production method with the use of a moth-eye mold uses a photocurable resin. Firstly, a photocurable resin is applied over a substrate. Then, an uneven surface of a moth-eye mold which has undergone a mold release treatment is pressed against the photocurable resin in vacuum, whereby the uneven structure at the surface of the moth-eye mold is filled with the photocurable resin. Then, the photocurable resin in the uneven structure is irradiated with ultraviolet light so that the photocurable resin is cured. Thereafter, the moth-eye mold is separated from the substrate, whereby a cured layer of the photocurable resin to which the uneven structure of the moth-eye mold has been transferred is formed over the surface of the substrate. The method of producing an antireflection film with the use of the photocurable resin is disclosed in, for example, Patent Document 4. The above-described moth-eye mold can be fabricated using an aluminum base, such as typically a substrate made of aluminum or a cylinder made of aluminum, or an aluminum film formed on a support that is made of a non-aluminum material, such as typically a glass substrate. However, in a moth-eye mold manufactured using an aluminum film formed on a glass substrate or plastic film, the adhesive property between the aluminum film (part of which is an anodized film) and the glass substrate or plastic film deteriorates in some cases. The applicant of the present application found that, by forming an inorganic underlayer (e.g., SiO2 layer) and a buffer layer containing aluminum (e.g., AlOx layer) on a surface of a base which is made of glass or plastic, the above-described deterioration of the adhesive property is prevented. This is disclosed in Patent Document 5. The applicant of the present application developed a method for efficiently producing an antireflection film using a moth-eye mold in the form of a cylinder (roll) according to a roll-to-roll method (e.g., WO 2011/105206). The moth-eye mold in the form of a cylinder can be formed by, for example, forming an organic insulating layer over an outer perimeter surface of a metal cylinder, forming an aluminum film on this organic insulating layer, and alternately and repeatedly performing anodization and etching on the aluminum film. In this case also, the adhesive property can be improved by forming the inorganic underlayer and the buffer layer disclosed in Patent Document 5. According to further researches carried out by the present inventors, an aluminum film formed on an organic insulating layer contains abnormal grains in many cases. The abnormal grains are formed by abnormal growth of a crystal of aluminum. The aluminum film is an aggregation of crystal grains whose average grain diameter (average grain size) is about 200 nm. On the other hand, the grain diameter of the abnormal grains is larger than the average grain diameter, e.g., not less than 500 nm in some cases. The organic insulating layer has a lower thermal conductivity than the other materials (metal materials and inorganic insulating films), and therefore, the aluminum film readily reaches a relatively high temperature in the process of depositing the aluminum film (e.g., sputtering or vapor deposition). As a result, it is inferred that abnormal growth of crystal grains is likely to occur, i.e., abnormal grains are likely to be produced. Note that such a phenomenon can also occur when an aluminum film is directly deposited on a surface of an aluminum pipe (e.g., the thickness is not less than 1 mm). When a moth-eye mold is manufactured using an aluminum film in which abnormal grains are present, structures corresponding to the abnormal grains are formed in the surface of a porous alumina layer of the moth-eye mold. When an antireflection film is formed using such a moth-eye mold, the structures corresponding to the abnormal grains are transferred to the surface of the antireflection film. Therefore, light is scattered by the structures transferred to the surface of the antireflection film which are attributed to the abnormal grains. That is, the antireflection film has a haze. In the case where the antireflection film is provided with an antiglare function as described above, no problem occurs in some cases even when the antireflection film has a haze which is attributed to the abnormal grains. However, there is such a problem that an antireflection film which does not have an antiglare function cannot be producing. Further, it is difficult to control the formation density (frequency of occurrence) of abnormal grains, and therefore, from the viewpoint of mass productivity, preventing production of abnormal grains is preferred. The present inventors disclose in the international patent application (PCT/JP2012/058394, WO 2012/137664) that an aluminum alloy layer which contains aluminum and such a metal element that the absolute value of the difference between the standard electrode potential of the metal element and the standard electrode potential of aluminum is not more than 0.64 V (for example, the metal element may be Ti, Nd, Mn, Mg, Zr, V, and Pb, and the content of the metal element in the entire aluminum alloy layer is less than 10 mass %) scarcely contains abnormal grains, and as a result, a mold can be obtained which is capable of producing an antireflection film that does not have an undesirable haze. The entire disclosures of Patent Documents 1, 2, 4, and 5 and the above-identified international patent application are herein incorporated by reference.
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Magnetic fields play an important role in a wide range of applications. They are used for instance in electric motors, dynamos and for signal transmission of radio or television. Furthermore, magnetic fields are used for medical diagnosis, where the most prominent example is magnetic resonance imaging (MRI). In each of these applications, the magnetic field is tailored to fulfill certain needs. For instance, in MRI, the formation of two field configurations is required: A spatially homogeneous and a linearly increasing gradient field. These special fields can be generated by electromagnetic coils, whereas the coil geometry and the applied current determine the field characteristics. For these simple field configurations, the optimal coil topology is well known. A homogeneous magnetic field is generated by a Helmholtz coil pair consisting of two identical coils that are placed symmetrically along a common axis, and separated by distance R equal to the coil radius. Each coil carries equal current owing in same direction. Similarly, a gradient field is generated by a Maxwell coil pair, which has the same topology but current owing in opposing direction and a larger coil distance of R√{square root over (3)}. Magnetic Particle Imaging (MPI) is an emerging medical imaging modality. The first versions of MPI were two-dimensional in that they produced two-dimensional images. Future versions will be three-dimensional (3D). A time-dependent, or 4D, image of a non-static object can be created by combining a temporal sequence of 3D images to a movie, provided the object does not significantly change during the data acquisition for a single 3D image. MPI is a reconstructive imaging method, like Computed Tomography (CT) or Magnetic Resonance Imaging (MRI). Accordingly, an MP image of an object's volume of interest is generated in two steps. The first step, referred to as data acquisition, is performed using an MPI scanner. The MPI scanner has means to generate a static magnetic gradient field, called “selection field”, which has a single field free point (FFP) at the isocenter of the scanner. In addition, the scanner has means to generate a time-dependent, spatially nearly homogeneous magnetic field. Actually, this field is obtained by superposing a rapidly changing field with a small amplitude, called “drive field”, and a slowly varying field with a large amplitude, called “focus field”. By adding the time-dependent drive and focus fields to the static selection field, the FFP may be moved along a predetermined FFP trajectory throughout a volume of scanning surrounding the isocenter. The scanner also has an arrangement of one or more, e.g. three, receive coils and can record any voltages induced in these coils. For the data acquisition, the object to be imaged is placed in the scanner such that the object's volume of interest is enclosed by the scanner's field of view, which is a subset of the volume of scanning. The object must contain magnetic nanoparticles; if the object is an animal or a patient, a contrast agent containing such particles is administered to the animal or patient prior to the scan. During the data acquisition, the MPI scanner steers the FFP along a deliberately chosen trajectory that traces out the volume of scanning, or at least the field of view. The magnetic nanoparticles within the object experience a changing magnetic field and respond by changing their magnetization. The changing magnetization of the nanoparticles induces a time dependent voltage in each of the receive coils. This voltage is sampled in a receiver associated with the receive coil. The samples output by the receivers are recorded and constitute the acquired data. The parameters that control the details of the data acquisition make up the scan protocol. In the second step of the image generation, referred to as image reconstruction, the image is computed, or reconstructed, from the data acquired in the first step. The image is a discrete 3D array of data that represents a sampled approximation to the position-dependent concentration of the magnetic nanoparticles in the field of view. The reconstruction is generally performed by a computer, which executes a suitable computer program. Computer and computer program realize a reconstruction algorithm. The reconstruction algorithm is based on a mathematical model of the data acquisition. As with all reconstructive imaging methods, this model is an integral operator that acts on the acquired data; the reconstruction algorithm tries to undo, to the extent possible, the action of the model. Such an MPI apparatus and method have the advantage that they can be used to examine arbitrary examination objects—e.g. human bodies—in a non-destructive manner and without causing any damage and with a high spatial resolution, both close to the surface and remote from the surface of the examination object. Such an arrangement and method are generally known and are first described in DE 101 51 778 A1 and in Gleich, B. and Weizenecker, J. (2005), “Tomographic imaging using the nonlinear response of magnetic particles” in nature, vol. 435, pp. 1214-1217. The arrangement and method for magnetic particle imaging (MPI) described in that publication take advantage of the non-linear magnetization curve of small magnetic particles. In the paper Weizenecker J. et al., “Magnetic particle imaging using a field free line”, J. Phys. D: Appl. Phys. 41 (2008) 105009, a simulation study on the use of a field free line (FFL) in magnetic particle imaging is presented. Further, a schematic setup of the simulated scanner geometry and the path of the FFL are described. The setup comprises a ring of 32 small coils (selection field coils) producing the rotating FFL. Two pairs of larger loops (drive field coils) move this FFL over the field of view. The diameter of the selection field coil ring is 1 m. Superimposing the selection field and the drive field, the FFL moves along the drive field vector, which over time has the form of a rosette, provided that the orientation of the FFL is always perpendicular to the drive field vector. Hence, the FFL scans back and forth while rotating slowly. This setup has, however, significantly higher power losses than the above described MPI apparatus exploiting the use and movement of a FFP and, hence, might not be realizable.
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Working towards an inclusive curriculum. The move towards an inclusive model of education presents teachers with the difficulty of differentiating the curriculum for children with speech, language and communication impairments. This paper focuses on the 'WiSaLT Curriculum Appendix'-a tool which can be used by teachers and speech and language therapists to help such children access the mainstream curriculum and to promote improvement in their language and communication skills. As well as highlighting potential areas of difficulty within each attainment target for key stage one, the appendix guides users to specific strategies and activities. Thus the speech and language therapist and teacher can identify which attainment targets might prove problematic for any one child and also have access to ideas which can help.
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Three thousand years ago on a battlefield in ancient Palestine, a shepherd boy felled a mighty warrior with nothing more than a stone and a sling, and ever since then the names of David and Goliath have stood for battles between underdogs and giants. David's victory was improbable and miraculous. Hehave won.Or should he have?In, Malcolm Gladwellchallenges how we think about obstacles and disadvantages, offering a new interpretation of what it means to be discriminated against, or cope with a disability, or lose a parent, or attend a mediocre school, or suffer from any number of other apparent setbacks.Gladwell begins with thestory of what happened between the giant and the shepherd boy those many years ago. From there,examines Northern Ireland's Troubles, the minds of cancer researchers and civil rights leaders, murder and the high costs of revenge, and the dynamics of successful and unsuccessful classrooms---all to demonstrate how much of what is beautiful and important in the world arises from what looks like suffering and adversity.In the tradition of Gladwell's previous bestsellers---anddraws upon history, psychology, and powerful storytelling to reshape the way we think of the world around us.
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Anton Pannekoek Institute for Astronomy Astronomer Joeri van Leeuwen receives Vici grant 26 February 2018 Astronomer Joeri van Leeuwen of the Netherlands Institute for Radio Astronomy (ASTRON)/UvA receives a Vici grant of 1.5 million euros to hunt for the source of gravitational waves. In the next five years he will study the afterglow of fused neutron stars with the radio telescopes in Westerbork, the Netherlands, with a team of six researchers. Gravitational waves occur when two heavy objects in the Universe, such as neutron stars or black holes, revolve around each other and merge together. With the instruments Virgo and LIGO it is already possible to detect these ripples in space-time. But where they come from, and how they are made, is still largely unknown. Van Leeuwen is able to study one of the causes of gravitational waves with the radio telescopes in Westerbork: the fusion of two neutron stars. 'Colliding neutron stars cause big explosions, which we can also see in radio light,' says Van Leeuwen. 'By studying the afterglow of these explosions, we can determine very precisely where the gravitational waves come from, which is not possible using gravitational wave detectors alone.' In October 2017, colliding neutron stars that caused gravitational waves were observed for the first time in different types of light with multiple telescopes. A special feature of the radio telescopes in Westerbork is that they can search an even larger part of the sky than other telescopes with the most sensitive widescreen cameras in the world (Apertif). By studying the neutron star explosions, Van Leeuwen also hopes to learn more about the matter of neutron stars. 'This matter is the same stuff that our bodies are made off, but we do not yet fully understand that. By measuring the afterglow of the explosions, we will learn more about the mass and the stability of the neutrons in the star.' Clashing neutron stars can also cause very energetic radio flashes. 'Neutron stars have very strong magnetic fields, and when they merge into a black hole, this magnetic field is thrown out, which is probably a super strong magnetic pulse that we might see as a radio burst with our radio telescopes.' The Vici grant allows Van Leeuwen to set up a new team of six researchers with whom he will hunt down the afterglow of gravitational wave sources. The observations start after the summer, when the Virgo and LIGO detectors start looking for gravitational waves again. 'As soon as they find one, we get a signal, and then we will try to find the source immediately with our telescopes.'
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Learning Redis is an example-based introduction which demonstrates how to work with the data store by creating a playable word game, written in Node.js. Fundamental topics of Redis are covered along the way. You’ll see how simple it is to install the database on your own machine or use a database provider in the cloud. Together we will discover the basic native data types of Redis and how to use them as we write a real game using JavaScript in a Node.js environment.We’ll store and retrieve data using the Redis CLI and understand the basic NoSQL data keys and storage techniques. Whether you’re writing a game or any other application, you need a place to store data. Learning Redis will demonstrate why you should implement Redis. Throughout the course, we will put to use the important concepts of Redis such as keys, values, sets, and hashes, which will help us build a solid application that works on some of the most important app requirements such as information storage, validation, pub/sub, notifications, and sorting. By the end of the course, you will understand how to make use of all of Redis’ features so you can design applications with rapid, efficiently managed data access. Who this course is for This course assumes a working knowledge of JavaScript; experience with Node.js is useful but not necessary. Viewers are not expected to be familiar with Redis, or NoSQL. What you will learn from this course Explore Redis commands and make the most of the supplied toolset Install Redis for use on a machine or on the cloud Use Redis interactively through its command line interface (CLI) Efficiently tackle application complexity using Redis data structures Store, list, and sort data with Redis to help create dynamic applications Make the most of the Redis data store by developing an exciting word game with Node.js
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New video reveals how flies land upside-down It’s not unusual to see a fly effortlessly stick an upside-down landing on a ceiling, but exactly how they pull off the aerial stunt has eluded scientists for decades. Even modern drones cannot compete with the fly’s sophisticated touchdown tricks. Now, a new study offers the most comprehensive exploration of fly landings to date, revealing agile maneuvers that could one day lead to robotic fliers that mimic the insect’s aerobatic abilities. In a bid to build machines that could imitate insect movements, Bo Cheng, a mechanical engineer at Pennsylvania State University in State College, started by scouring 50 years of scientific literature for studies involving fly landings. He was surprised that such a common occurrence was so underdocumented. Then he realized why: The flies’ lightning-quick moves during landings aren’t easy to observe. So, Cheng and colleagues used high-speed video to capture and analyze more than 20 bluebottle flies (Calliphora vomitoria), known for their exquisite maneuvers, sticking their inverted landings in a flight chamber. The flies landed in versatile ways. Some stuck the landing by first planting their forelegs on the surface, then swinging their bodies into place, similar to a back flip (see video, above). Other landings looked more like barrel rolls. After taping 18 perfect landings, the team discovered that flies depend primarily on visual cues to make these maneuvers. When a fly sees that it’s about to collide with a ceiling, for example, it must decide in 50 milliseconds how to turn upside down and grab the ceiling with its feet, Cheng and colleagues write today in Science Advances . But even nimble flies blunder: The study also describes 15 failed landings, which reveal that the insects need to move in a specific range of motion in less than the blink of a human eye to achieve a perfect landing and avoid colliding with the ceiling. “This is a really interesting new paper,” says Jessica Fox, a biologist studying insect sensory systems using high-speed video at Case Western Reserve University in Cleveland, Ohio, who was not involved in the study. However, the insects’ landings may have been influenced by the experimental setup, she adds. Flies were stimulated with mechanical vibrations to get them to take off—in an area the size of a small box. If they had more room, and if they weren’t frightened into taking off, they may have chosen easier landings, she says. The study shows “what flies can do at their limits, when they are flying fastest and need to make decisions in the shortest amount of time.” The flies “are just a starting point” in exploring how they and other flying insects—from mosquitoes to bees—control their complicated maneuvers, says co-author Sanjay Sane, an integrative biologist at the National Centre for Biological Sciences in Bengaluru, India. More studies of this kind will help scientists start to pinpoint the most important shared flight maneuvers across species, he says. And once scientists know more about the processes that control fly landings, Cheng adds, they may discover how to create robots that mimic the flies’ barrel rolls and other fly feats. “Just like children mimic their parents, we can let the fly teach a robot.”
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The present invention relates to the field of computer graphics. Many computer graphic images are created by mathematically modeling the interaction of light with a three dimensional scene from a given viewpoint. This process, called rendering, generates a two-dimensional image of the scene from the given viewpoint, and is analogous to taking a photograph of a real-world scene. As the demand for computer graphics, and in particular for real-time computer graphics, has increased, computer systems with graphics processing subsystems adapted to accelerate the rendering process have become widespread. In these computer systems, the rendering process is divided between a computer's general purpose central processing unit (CPU) and the graphics processing subsystem. Typically, the CPU performs high level operations, such as determining the position, motion, and collision of objects in a given scene. From these high level operations, the CPU generates a set of rendering commands and data defining the desired rendered image or images. For example, rendering commands and data can define scene geometry, lighting, shading, texturing, motion, and/or camera parameters for a scene. The graphics processing subsystem creates one or more rendered images from the set of rendering commands and data. Graphics processing subsystems typically use a stream-processing model, in which input elements are read and operated on by successively by a chain of stream processing units. The output of one stream processing unit is the input to the next stream processing unit in the chain. Typically, data flows only one way, “downstream,” through the chain of stream processing units. Examples of stream processing units include vertex processors, which process two- or three-dimensional vertices, rasterizer processors, which process geometric primitives defined by sets of two- or three-dimensional vertices into sets of pixels or sub-pixels, referred to as fragments, and fragment processors, which process fragments to determine their color and other attributes. Typically, the rendering commands and data sent to the graphics processing subsystem define a set of geometric primitives that are potentially visible in the final rendered image. The set of potentially visible geometric primitives is typically much larger than the set of geometric primitives actually visible in the final rendered image. To improve performance, the graphics processing subsystem can perform one or more visibility tests to determine the potential visibility of geometric primitives. Using the results of these tests, the graphics processing subsystem can remove, or cull, geometric primitives that are not visible from the set of potentially visible geometric primitives, thereby reducing the number of geometric primitives to be rendered. Previously, visibility testing and culling of geometric primitives, referred to as culling operations, were performed in the setup and rasterization units of the graphics processing subsystem. As rendered scenes become more complex, they typically include a large number of small geometric primitives. The increasing number of geometric primitives tends to create processing bottlenecks in the setup unit. Additionally, the vertices associated with each geometric primitive can include a set of attributes used for rendering. The bandwidth required to communicate vertices and their associated attributes to the setup unit creates further processing bottlenecks. This problem is exacerbated by the increasing number of attributes associated with vertices to perform complex rendering operations. It is therefore desirable to perform culling operations as soon as possible in the graphics processing subsystem to decrease wasteful rendering operations, to reduce the bandwidth requirements for communicating vertices and associated attributes, and to improve rendering performance. It is further desirable to reduce processing bottlenecks in the setup unit without substantially increasing the complexity of other portions of the graphics processing subsystem.
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Only a few days left to Double your gift Forget offshore oil drilling. NASA’s working on a project that would generate clean, renewable offshore energy, by growing algae in floating plastic bags. These floating algae farms would take in wastewater from treatment plants. For algae, wastewater is like the nectar of the gods: The ammonia and phosphates act as a fertilizer. So the algae would float happily contained in the baggies, getting fat with lipid oil, and cleaning up the wastewater in the process. Eventually, the algae farmers would harvest the oil, recycle the plastic and start all over again. There are a few benefits to this fuel system. It takes less land then algae farms, it recycles wastewater, and it avoids the energy-intensive cooling and the problems with evaporation that open algae ponds have to deal with. And if these offshore energy sources spilled, the algae shouldn’t cause too much harm. The plastic bags might be expensive to replace, but the algae would die quickly in the saltwater. But the system does require a lot of plastic — about two square miles to create 2.4 million gallons of algae oil per year. According to Technology Review, the NASA researchers who came up with the idea aren’t totally sure what they’d do with all that algae-covered plastic after they were done using. Imagine miles and miles of mildewy shower curtains and you get some idea of the issue. Still, there’s nothing new about having too many plastic bags and no perfect way to dispose of them. But right now they mainly hang around in trees bothering Liz Lemon, when they could be generating renewable fuel. See: NASA Wants to Launch Floating Algae Farms, Technology Review
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Deterrent behaviour is normal, necessary and acceptable as long as the dog stops when the animal or person backs off. You’ll commonly see adult dogs use deterrent behaviour to warn off or discipline unruly pups or dogs with poor social skills. Although deterrent behaviour is widely accepted in humans, we often don’t afford dogs the same right to communicate their discomfort. Aggression is simply communication. The burning question is where acceptable communication crosses the line into unwanted aggression. For perspective let’s take a look at the ACTT K9 Communications Continuum. Think of canine communication and aggression on the same continuum. In Zone-A, you’ll see normal, healthy communication. Zone-B is where the intensity starts to escalate. Social and confident dogs exist in Zone-A. Under-socialized and fearful dogs live in Zone-B. On a best day scenario when anxiety is low, B dogs live in the center of the continuum and start communicating their discomfort with deterrent behaviour. That’s why they’re perceived as reactive or dogs with a low threshold. A dog can change its communication according to the situation by sliding up and down on the continuum with the intent to prevent conflict. The dog may communicate its discomfort with calming signals in Zone-A, but if those signals aren’t respected the dog’s behaviour will move toward Zone-B into deterrent behaviour. The line between A and B is where the dog flips from mild to more severe deterrent behaviour leading to fear and aggression. Reprimands cripple communication causing the dog to quickly jump to severe behaviour in order to avoid the admonishment. Punishing or allowing severe deterrent behaviour can create an aggressive bully that picks fights. When communication is repeatedly punished it creates a learned helplessness and can trigger a primordial survival instinct manifesting in self-defense behaviours. To prevent or mitigate aggression and shape a confident dog that’s a master communicator: Learn to interpret canine body language Encourage natural communication Teach acceptable deterrent limits The secret to solid communication is socialization and because it’s a skill, the “use it or lose it” rule applies. Dogs should be carefully and thoroughly socialized before four months of age and socialization should continue throughout their lives to keep their skills fine-tuned and prevent aggression.
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7 Effective tips how to leave healthy life Eating is the most basic and fundamental way of obtaining nutrients from the outside world into the body. These nutrients are used by the body for growth and development including the development of your immune system. However, to get the best nutrients, you must know the right food and amount you need to take for growth and development to take place effectively. That is exactly what this article is all about. If you have been looking for healthy eating tips, here are seven of them, read on! 1. Base your meals on carbohydrates Carbohydrates, also known as energy giving foods should always be included in your meals. Such meals that provide enough starch include bread, rice, pasta, and noodles to mention a few. Whole grains that contain fibre is also good for the digestion of food. It is advisable to obtain half the calories you get from carbohydrates rather than from fats. 2. Consume a variety of Foods Different nutrients have different importance in the growth and development of the body. You, therefore, need a variety of such nutrients to ensure that growth in your body takes place effectively. Apparently, your body needs more than 40 different nutrients to ensure good health full functionality. You need vitamins for improved immunity, proteins to build your body and carbohydrates to give you energy. 3. Include fruits and vegetables in your meals Fruits are a great source of vitamins. As stated earlier, your body needs vitamins to improve its immunity from disease-causing germs. Consumption of fruit when having a meal is a good way of implementing a culture of eating fruits. Most people overlook the importance of eating fruits without knowing the actual benefits of doing so. Vegetables are also a great source of plant vitamins and minerals that aid the process of naturally immunizing the body. 4. Cut the consumption of fats and sugar While we should consume some fats for the various importance like provision of fatty acids, we should limit our consumption to prevent gaining weight. Weight is easily gained from the consumption of fats since they provide more than twice the amount of calories we get from carbohydrates. The good news is, we still can get the necessary fatty acids from substitute fats like vegetable oil, nuts, avocados, and oily fish rather than from cream, cheese, and butter. A lot of sugar is known as the major cause of tooth decay and increased calories. Manage the consumption at a low level. 5. Eat regularly but moderately Having every meal at the right time is good for the development of the body. Skipping meals or consuming them at delayed times is discouraged since the increased hunger pangs will lead to rapid eating without concentration of what you are consuming. Learn to keep your portions moderate. In cases of plenty of food, share with someone. 6. Drink plenty of water Water forms a large percentage of our bodies. During the day, when in our everyday businesses, we lose a lot of water through dehydration. As such, it is mandatory that we replace the lost water by drinking at least 1.5 litres per day. Other drinks like soft drinks, milk coffee, and tea can also add water levels in our bodies. 7. Do a lot of Exercises A lot of junk calories in our bodies can lead to increased weights and increase the risk of heart-related problems. To ensure that you burn any extra calories, engage in physical activities on the field or indoors that will get you sweating. Include an average of 75 minutes into your daily schedule for physical exercises. It is also good for blood circulation.
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April 19, 2012: Last month, when the sun unleashed the most intense radiation storm since 2003, peppering satellites with charged particles and igniting strong auroras around both poles, a group of high school students in Bishop, California, knew just what to do. They launched a rubber chicken. The students inflated a helium balloon and used it to send the fowl, named "Camilla," to an altitude of 120,000 ft where she was exposed to high-energy solar protons at point blank range. Many space enthusiasts are already familiar with Camilla. She's the mascot of NASA's Solar Dynamics Observatory. With help from her keeper, Romeo Durscher of Stanford University, Camilla corresponds with more than 20,000 followers on Twitter, Facebook, and Google+, filling them in on the latest results from NASA's heliophysics missions.
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. So, towards the end of wavelet us, we have to understand uh the following that there is a resolution that is happening at different scales right and there is a resolution in time. And what about in the frequency is a resolution the same in frequency right, I mean imagine I have have a short burst of a pulse right. And I can measure the the burst or I can measure some event in the a of the signal in and the variance of the signal in in in in time and some statistical properties of the signal in time, and can I have the same sort of resolution that I can get in the frequency domain. So, this is one of the questions that one would naturally think about. So, fortunately for us somebody did investigation on this time frequency uncertainty principle. This follows a kin to the the position momentum uncertainty Heisenberg's uncertainty principle that we are aware in quantum mechanics right. And the same sort of idea is exists actually in in in when we look at time frequency uncertainty in signal processing. And there is a more deeper theory using operators in mathematics and will not get there ok. So, let us begin consider a finite energy signal right. If it is a finite energy signal which means integral minus infinity to plus infinity, I mean you can put any range for this, I mean this is very general, I mean you really will not ideally reach minus infinity and plus infinity, but this is just for pedagogical purposes and if you see some range or you just have to put the appropriate range here in your definite integral. So, this energy is strictly less than infinity . Now, let us assume that the signal is centered around 0 I would say precisely at 0 both in time and frequency, that is it is 0 mean if it is not 0 mean you can always subtract the bias and get it to 0 mean ok. Now, when we think about signals we discussed in the very beginning of module 1, when we looked into signal geometry, that we can think about different kinds of averaging statistics 1 is just a normal time average youre given the samples you compute all these statistics, whether it is mean or the variance or second moment third moment so on and so forth right. You can compute all the moments across the signal or you could do the statistical average right statistical average. So, let us look at the time average time average ok. Now, let us compute the variance in time and frequency by usual time averaging ok. Now since we said we are dealing with 0 mean we can compute the variance in time sigma t square, as integral minus infinity to plus infinity t square mod s of t square dt and there is a normalization factor here, which is the square of the l 2 norm of the signal right. And why should we do this is a question that you might want to ask why should I normalize? And, if we treat the signal as a random signal there should be some distribution over which we have to weigh it right. So, if you take if you fold this norm inside right. So, if you can you can you can basically rewrite this as essentially integral minus infinity to plus infinity t square mod of s of t square dt divided by the l 2 norm . Now can you appreciate that this is like like your density right this is like your like your PDF probability density function, because when you integrate this this this is basically this integrates to 1 right. So, therefore, you can compute a moment a second moment like this ok. Now, we will do this in frequency computing the variance in the frequency domain, we get sigma omega square is integral minus infinity to plus infinity omega square modulus of s of omega square d omega divided by the norm l 2 norm over the spectrum right. Again you can interpret this as a density like what we did earlier right there is no big deal. So, this is also like you can interpret this as ok. So, now, I think we are sort of set with our with our with our problem. Now, you can also think about in the notion of quantum mechanics, you can think about this as position this is momentum and you can think about these operate or these quantities and you are also looking at the variance here right or some other 2 set of quantities. Now, by Parseval's theorem from your undergraduate norm s of t squared l 2 norm of s of t is the same as s of omega square right. Because, if you apply the Fourier transform you are not going to alter the energy in the signal, otherwise it would be the transformation is useless if if you lose the energy right, because of energy conservation property . So, notation wise this is easy for me I can just write it like this, some norm of s square I will get rid of t and omega I am saying norm of s square because it is the same whether it is time or frequency ok. Now, let us consider the following product, which is the variance in time and the variance in frequency I consider this product . This is essentially integral minus infinity plus infinity t square mod s of t square dt times. Now, we can interpret the omega times modulus of s of omega as this quantity, because from duality if you take d by dt of s of t in the frequency domain, it is you are multiplying by g omega right and the modulus will pull the magnitude of j to be one right and you have omega square s of omega square modulus of s of omega square right. So, this is an important step divided by power 4, because you have a norm s square for this term and another norm s square for this term. So, you have a power 4 in the denominator and in this quantity it is basically due to Fourier transform property right take the Fourier, it is j omega right. So, you have this additional jmo this j omega quantity which justifies what we have. So, now, consider integral minus infinity plus infinity modulus of I will say t square times s of t square dt consider this this can be written I can fold the t inside the modulus there is no problem with it. So, I can write this in this form modulus t times s of t square dt. And you can interpret this quantity as the l 2 norm square of t time's s of t ok. See how we are kind of building the the logic right from starting from the variance to interpreting this into the norm. And, similarly integral minus infinity to plus infinity modulus of d by dt s of t square dt can be interpreted as the l 2 norm of the derivative of the signal right, l 2 norm square of the derivative of the signal . Now, we have a product of 2 norms. So, your intuition should tell that there is Cauchy Schwartz somewhere kicking in ok. So, let us apply Cauchy Schwartz inequality . So, the reason states that if you look at the norm of 2 functions, that are possibly complex then the modulus of the in the product square is basically less than or equal to the norm square of the product of the individuals ok. Now, using this we can say and say this is relationship a using A, we can write sigma t square times sigma omega square as a quantity, which is greater than or equal to because now it is existing in product form exactly. So, therefore, the inequality is this way right one over norm of s l 2 norm of s power 4 times I bring the modulus integral minus infinity to plus infinity t times s of t times there is one careful observation, that you have to make where I am bringing in the conjugate of this signal under the hermitian inner product form . Now, this quantity that we have modulus of some integral square so, this is this can be a complex quantity. So, we can simplify this little carefully. So, this is one over the norm of s power 4 times I can write the absolute value of the real part of integral t times s of t times d by dt of s of t bar dt square why? Because, you know for complex numbers modulus of real of z is certainly less than or equal 2 modulus of z right. This is a straight forward result. So, you take just for a cross check 3 plus 4 j is that vector the length is 5, then the real is 3 and when the complex part is 0 then it coincides with equality. So, you you have this relationship . Now, real part of some complex quantity z can be written as one half z plus z conjugate, this is a straight forward result . Now consider the real part of this integral minus infinity to plus infinity t times s of t times derivative of the signal conjugate dt right . I can write this as 1 half I will pull the t factor outside because it is just a scalar it is time variable it is a scalar right . So, we can write it as s of t times derivative of s bar of t plus s bar of t derivative of s of t right using this this room using this step one half of of z plus z conjugate I just did that yeah right. So, I just take this as my z here I just conjugate it I will know I will come to the point I am just yeah I need the integration there yes a real part . So, I just have t times I just I am looking at this term here I am just rewriting this thing here and I just have to put if you are ok with I am just focusing on this term just the argument of the of the integral ok . Now, let us focus on the term within the integral let us focus on the term within the integral . So, this is basically I would say term within the integral is basically half t times d by dt of modulus of s of t square why? Because, you can write modulus of s of t is s of t is power of t now you take the derivative using chain rule and it automatically comes ok. So, therefore, sigma t square times sigma omega square is greater than or equal to now I have to square this quantity right if it is one-fourth, I have a norm s power 4 and then have an absolute value here then this integral minus infinity to plus infinity t times d by dt of modulus of s of t square dt . Now, still it looks complicated let us consider integral minus infinity to plus infinity t times derivative of modulus of s of t square dt and perform integration by parts right. We have the familiar this is what I recall from my high school I late this is a inverse function logarithmic. So, on and. So, forth right you you use that last is exponential. So, you apply this rule integration by parts . So, what we get is t times s of t square minus infinity to plus infinity minus integral, because I take the derivative I integrate that I get this and then I take a differentiate time, then I get one there right first function integral or second function minus integral of second function derivative of the first function ok. Now, this quantity goes to 0 and this is basically interpretable as negative norm of s square . Therefore, sigma t square times sigma omega square is greater than or equal to 1 upon 4 times minus norm s square and if you square this quantity because I have that modulus of that integral square is what I have. So, this is basically just 1 by 4, because norm s power 4 and norm s power 4 cancel in the numerator and denominator right. It is a very interesting result, I mean it is a very interesting result that you look at the variance in time and the variance in frequency and and that is lower bounded by 1 upon 4 take any signal take any signal any s of t. It is at least this much that you will live with your uncertainty in your measurement in time and your measurement in in frequency, it is a very very profound ah profound result and this result was proved by no less than the Nobel prize winner Dennis Gabor who is the father of holography. So, let us say the roots this this is originally proved by Dennis Gabor in 1946 and of course, Dennis Gabor was great in many areas including in signal processing the signal processing result, but of course, he is a Father of Holography . So, now we have a very important principle uncertainty inequality or uncertainty principle in signal processing, that we cannot simultaneously localize in time and frequency no matter what? So, a follow up question arises when does this equation when when is the inequality is satisfied with equality or when is the equality satisfied, when can we get this actual limit of 1 by 4. So, for this we asked the next question when can we achieve equality that is sigma t square, sigma w square, sigma omega square, equals one-fourth we need to I need to get to this lower bound . Now fortunately we have a solution from Cauchy Schwartz again that we are comfortable, we can say it happens when t times s of t is some constant k times derivative of s of t and I assume at the moment I just will remove the conjugation here and I will just assume s of t assuming real signals. Now the k is this factor right I mean when this k times the derivative of s of t, then this is equal the inequality becomes a equality right. Now, we have a differential equation here. So, let us group the terms and integrate both sides . So, how we do this we say derivative of s of t by s of t is t upon k times dt and then I need to do an integration on both the sides ok So, if I integrate I get log s of t is t square upon 2 times k plus some constant of integration . Now, s of t is of the form e power t square upon 2 k plus some constant, which is if you write it carefully it is e power times c times e power t square upon 2 k let me call this as some constant a times e power t square upon 2 k well we have done the integration, but let us see if things are making physical sense for us right. So, if you recall in the very beginning I said let us consider finite energy signals. Now I have a solution s of t is of this one a times e power t square by 2 k and if you if you let k to be a positive constant the energy in s of t would be infinite potentially it could be infinite right. So, therefore, if s of t is to be a finite energy signal, then k must be a negative real number ok. So, therefore, let b equals minus k right let b is some negative k. So, if I did that then s of t is some a times e power minus t square by 2 b . Now, this is easy for us to think about because this is like has the form of a Gaussian pulse, you are not making it a distribution I mean if you if you want if you can choose a to be one upon root of 2 pi b, then it becomes like a distribution t degrades to one otherwise this is just a Gaussian pulse . Now, this basically led to Gabor transformations. So, this is form this form led to Gabor transforms I mean I am not going to deal with Gabor Gabor transforms, I am not going to deal with Gabor's Gabor's transforms, if we were to go people to go into into more details of time frequency analysis we would start possibly with this as our first step and then go into the details ok. So, but and you can also appreciate ah why you think about the Fourier transform of a Gaussian pulse why this has the same, shape? And Gaussian has very interesting consequences one of this is this uncertainty relationship, the Gaussian PDF has the maximum uncertainty. If you if you look at the differential entropy right and evaluate this for the Gaussian PDF it gives you the maximum uncertainty right. And that is the reasons why you look people look into Gaussian PDFs you know when they are in their study of signals with noise and particularly noise having Gaussian PDF. And Gaussian PDF again comes from your central limit theorem results. So, somehow whether it is consequential or it just nature is providing you that way it is just there there are a lot of very interesting properties with Gaussian, whether it is distribution or a pulse or a transform or whatever it is and you see this again and again in signal processing and information theory ok. So, we will so, we will we will stop at this stage I think this is something which you have to really understand. And, before we conclude I would sort of give you a homework problem to ponder ponder on how the time frequency uncertainty principle applies, in the context of wavelet decomposition at different scales . So, we have studied the wavelet decomposition and reconstruction. So, at every stage of wavelet decomposition we have a certain resolution right, it is a time resolution. Now think about if this transformation can meet this this bound or how close or how far away is it from the uncertainty principle, if you were to do localization through wavelet us ok this is something to think about this may or may not appear on the exam, but this is a hint for you to think through this homework exercise. So, we will stop here and we can go to questions ok.
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Q: Why is -(int) int being any int value ,an r-value? #include<stdio.h> int main() { int i = 10; printf("%d", ++(-i)); return 0; } This is obviously an Compilation Error as post(pre)increment/decrement take l-values. So in this case -i is r-value BUT how and why? A: The preincrement operator ++ (and other similar operators) requires an lvalue, which is an expression that not only has a type/value but also refers to an object. Roughly speaking, lvalues are things you could put on the left hand side of the = operator (but there are some exceptions) or put after the & (address-of) operator (but there are some exceptions here too). The term rvalue is slang (not defined by the language standard) for expressions which are not lvalues. In the case of -i, i is an object, but there is no object -i; -i is just the resulting value from negating the value of i. Assigning something to -i is not possible because there is no object/storage it refers to.
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1.. Introduction ================ Virions (infectious virus particles) are nano-sized carriers of information whose objective is to infect a host cell and generate progeny that can, in turn, repeat the infection cycle. When traveling outside of the host cell, virions may encounter harsh environmental conditions. Knowledge of the deformability (stiffness, *k*), the energy required for mechanical failure (toughness, *T*), and the limits to fatigue for virions has been acquired through studies using atomic force microscopy (AFM), but mainly for viruses that do not have an internal membrane.[@cit1]--[@cit4] The mechanical properties of these virions ultimately recapitulate the molecular interactions across the viral icosahedral shell.[@cit5],[@cit6] There is no comparable information available for icosahedral virions in which an internal membrane vesicle surrounds the densely packaged DNA and, to our knowledge, such viruses with RNA genome are yet to be identified. Defining how a membrane and capsid provide protection to the genome within will provide new insights into the function and properties of biological materials, thereby inspiring the design of novel nanostructures. PRD1, the prototype for icosahedral dsDNA viruses with an internal membrane, is a large and complex enterobacterial virus (family *Tectiviridae*; ∼65 nm mean diameter and triangulation number pseudo-*T* = 25, [Fig. 1a](#fig1){ref-type="fig"}). Its crystal structure revealed the molecular interactions across the major capsid proteins (MCPs) P3 (395 residues) and with the membrane.[@cit7],[@cit8] P3 trimers (capsomers) are arranged in the group of nine (GON) layout in the virion facets (Fig. S1a[†](#fn1){ref-type="fn"}). The minor capsid protein P30 cements the edges of the icosahedron. Eleven of the twelve vertices are capped by peripentonal P3 trimers and by spike complexes[@cit7]--[@cit11] ([Fig. 1a](#fig1){ref-type="fig"} and S1a[†](#fn1){ref-type="fn"}). The internal membrane enclosing the densely packaged dsDNA is composed of a roughly equal mass of lipids and membrane proteins.[@cit8] The twelfth vertex is the unique, membrane-embedded portal used for DNA packaging into the procapsid and later for DNA ejection *via* the formation of a proteo-lipidic tube.[@cit12],[@cit13] ![(a) Schematic of PRD1 highlighting the main structural features of the virus particle. (b) Protein composition of wt PRD1 and subviral particles analysed by SDS-PAGE and Coomassie staining. Left: Molecular masses (M; kDa). Right: Positions of the most abundant proteins; the vertical black line refers collectively to membrane proteins (MPs, including P14, P16, P18, P20, P22, P31 and P32). Cementing protein P30 identified in the P3-shell by mass spectrometry is indicated by a black arrowhead. (c--f) Atomic force micrographs of wt PRD1 and subviral particles with scale bar (100 nm) and *z* range (75 nm) indicated in (f). (c) Wt PRD1 featuring different particle orientations. Inset: Crystal structure of wt PRD1.[@cit7] Yellow, green, cyan and blue denote the P3 pseudo-hexameric capsomers composing the icosahedral asymmetric unit; white lines delineate a virus facet; white pentagons, triangles, and ovals indicate icosahedral 5-, 3- and 2-fold symmetry axes, respectively; (d) Sus1 procapsids (no DNA within). Arrowheads indicate the visible depression due to the missing packaging portal in the unique vertex. Inset: Schematic of Sus1 procapsid; (e) P3-shell. Arrowheads highlight the depressions visible at all vertices due to the absence of the peripentonal capsomers and vertex complexes. Right inset: The star-shaped vertex depression at higher resolution (*z* range: 15 nm). Left inset: Schematic of P3-shell. Arrowheads indicate some of the de-capped vertices. (f) DNA-filled vesicle. Inset: Schematic of vesicle represented as an icosahedron for clarity and consistency with the wt PRD1 schematic representation -- this shape, however, might not be retained in the purified membrane-vesicle.](c8nr00196k-f1){#fig1} Guided by the available genetic, biochemical, and structural information, we chose to utilize (i) wild type PRD1 (wt PRD1), (ii) a PRD1 mutant that forms procapsids devoid of DNA (Sus1 procapsid), (iii) the icosahedral P3-shell composed of MCP P3 and the minor capsid protein P30 ([Fig. 1b](#fig1){ref-type="fig"} and Table S1[†](#fn1){ref-type="fn"}), but lacking the pentons and peripentonal capsomers (P3-shell), and (iv) proteo-lipidic membrane vesicles enclosing a complete genome (vesicle; [Fig. 1b](#fig1){ref-type="fig"}). We used AFM to examine the mechanical responses of these particles in an aqueous environment by assessing their stiffness and yield behaviour under an applied force and used finite element modelling, where possible, to aid the analysis. 2.. Experimental ================ 2.1. PRD1 specimen production ----------------------------- Wt PRD1 and mutant PRD1 and mutant *sus1* \[amber mutation in gene *IX*\] were propagated on *Salmonella enterica* serovar Typhimurium strain DS88 or on suppressor strains PSA(pLM2) or DB7156(pLM2).[@cit14]--[@cit18] Cells were grown in Luria--Bertani (LB) medium at 37 °C. For the production of wt and mutant phage particles, DS88 cells were infected using a multiplicity of infection of 8--10. For mutant particle production, infected cells were collected 15 min after infection (Sorvall rotor F12, 5000 rpm, 10 min, 22 °C) and transferred to a fresh pre-warmed medium. Virus particles were purified by polyethylene glycol--NaCl precipitation and rate zonal ultracentrifugation in sucrose (Sorvall rotor AH629), as previously described.[@cit19] For AFM, wt PRD1 and Sus1 procapsids were further purified by equilibrium ultracentrifugation in sucrose (Sorvall rotor AH629). The particles were concentrated by differential centrifugation (Sorvall rotor T647.5, 32 000 rpm, 2 h, 5 °C). A buffer containing 20 mM potassium phosphate pH 7.2 and 1 mM MgCl~2~ was used for purification and resuspension. For P3-shell preparation, the rate zonal purified Sus1 mutant particles (2 mg ml^--1^ in 20 mM Tris-HCl, pH 7.2, 1 mM MgCl~2~) were treated with 1% (w/v) sodium dodecyl sulfate (SDS) for 15 min at 25 °C.[@cit20] P3 shells were isolated by rate zonal centrifugation in a linear 5--20% (w/v) sucrose gradient using the Tris buffer (Sorvall rotor AH629, 24 000 rpm, 1 h 45 min, 20 °C). The particles were concentrated by centrifugation (Sorvall rotor T865, 34 000 rpm, 4 h, 5 °C) and resuspended in Tris buffer. For membrane vesicle preparation, the rate zonal purified Sus607 particles devoid of the major membrane protein P11 (1 mg ml^--1^ in 20 mM Tris-HCl, pH 7.2) were treated with 2.5 M GuHCl[@cit21] and membrane vesicles were purified by equilibrium centrifugation in a linear 20--70% (w/v) sucrose gradient (Sorvall rotor TH641, 22 000 rpm, 16--18 h, 20 °C). Protein concentrations were determined by Bradford assay.[@cit22] Particles were analyzed using sodium dodecyl sulfate polyacrylamide gel electrophoresis[@cit23] (SDS-PAGE; 16% acrylamide; [Fig. 1b](#fig1){ref-type="fig"}). Virus particles were stored at 4 °C for no more than 4 weeks. During this time, more than 95% of the wt PRD1 particles remained intact and without the loss of their genome as visualized by cryo-electron microscopy (cryo-EM) 2D imaging \[a JEM-2200FS (JEOL) transmission electron microscope equipped with an UltraScan 4000 SP 4k × 4k camera (GATAN)\] (Fig. S2[†](#fn1){ref-type="fn"}). Sus1 procapsid, P3-shell particles and vesicles were similarly stored and also used within this time frame (Fig. S2[†](#fn1){ref-type="fn"}). 2.2. Protein identification by mass spectrometry ------------------------------------------------ Silver stained[@cit24] protein bands were cut out of the polyacrylamide gel and "in-gel" digested. Cysteine bonds were reduced with 0.045 M dithiothreitol (Sigma-Aldrich, USA) for 20 min at 37 °C and alkylated with 0.1 M iodoacetamide (Fluka, Sigma-Aldrich, USA) at room temperature. Samples were digested by adding 0.75 μg trypsin (Sequencing Grade Modified Trypsin, V5111, Promega) overnight at 37 °C. After digestion, peptides were purified with C18 microspin columns (Harvard Apparatus) according to the manufacturer\'s protocol. The dried peptides were reconstituted in 30 μl of buffer A \[0.1% trifluoroacetic acid (TFA) in 1% acetonitrile (ACN)\]. Liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS) analysis was carried out on an EASY-nLC1000 (Thermo Fisher Scientific, Germany) connected to a Velos Pro-Orbitrap Elite hybrid mass spectrometer (Thermo Fisher Scientific) with a nano-electrospray ion source (Thermo Fisher Scientific). The LC-MS/MS samples were separated using a two-column setup consisting of a 2-cm C18-Pepmap trap column (Thermo Fisher Scientific), followed by a 15-cm C18-Pepmap analytical column (Thermo Fisher Scientific). The linear separation gradient consisted of 5% buffer B in 5 min, 35% buffer B in 60 min, 80% buffer B in 5 min and 100% buffer B in 10 min at a flow rate of 0.3 μl min^--1^ (buffer B: 0.1% TFA acid in 98% acetonitrile). Six microliters of sample were injected per LC-MS/MS run and analyzed. Full MS scan was acquired with a resolution of 60 000 in the normal mass range in an orbitrap analyzer and followed with CID-MS2 top 20 most intense precursor ions within the ion trap (energy 35). Data were acquired using LTQ Tune software. The acquired MS2 scans were searched against the enterobacteria phage PRD1 (NCBI) protein database using the Sequest search algorithms in Thermo Proteome Discoverer. The allowed mass error for the precursor ions was 15 ppm and for the fragment 0.8 Da. A static residue modification parameter was set for carbamidomethyl +57 021 Da (C) of the cysteine residue. Methionine oxidation was set as dynamic modification +15 995 Da (M). Only full-tryptic peptides were allowed for the maximum of one missed cleavage. 2.3. Surface preparation and immobilization of PRD1 particles ------------------------------------------------------------- Freshly cleaved surfaces (∼1 cm^2^) of mica (Ted-Pella Inc., CA, USA) were functionalized with 3-(2,2-aminoethylamino)-ethylaminopropyltrimethoxysilane (APTES; Sigma-Aldrich) by adapting a previously described procedure.[@cit25] Briefly, mica was left to incubate with 30 μL of APTES in a 4 l gas incubator for 2 h. A small amount of water (10 μl) was deliberately added to generate a root-mean-square surface roughness of 1.7 to 2 nm, which proved beneficial to particle attachment. Following the APTES functionalization, surfaces were covered with 100 μl Hepes buffer (10 mM HEPES, pH 7.4, 150 mM NaCl, 2 mM MgCl~2~) containing ∼10 μg virus particles (wt PRD1, Sus1 procapsid, or P3-shell). PRD1 vesicles were attached to freshly cleaved mica instead of APTES-coated mica. Virus particles were allowed to adhere for 30 min, and excess particles were removed by washing with buffer. 2.4. AFM imaging and nanoindentation ------------------------------------ All PRD1 particles were found to attach as a monolayer to the prepared mica surfaces that could be readily visualized by AFM. Imaging and nanoindentation measurements were carried out using a MultiMode 8 AFM with a Nanoscope V controller (Bruker, CA, USA) at room temperature in Hepes buffer. Wt PRD1, Sus1 procapsids, and P3-shells were analysed with sharpened triangular Si~3~N~4~ cantilevers with a nominal spring constant of 0.7 N m^--1^ (ScanAsyst-Liquid; Bruker). For PRD1 vesicles, Si~3~N~4~ cantilevers with a nominal spring constant of 0.1 N m^--1^ (AC40; Bruker) were used. The real spring constants of the cantilevers were measured using the thermal noise method[@cit26] as implemented in the NanoScope software and were found to be close to the nominal values. Imaging was performed in Peak Force Tapping mode, with a typical tapping amplitude of 40 nm and a driving frequency of 2 kHz. For wt PRD1, Sus1 procapsids, and vesicles, the peak force was usually 100 pN; for P3-shells, it was 80 pN. Under these conditions, the image quality was sufficient to reliably identify the virus particles (and in some cases, their orientation and surface sub-features), and in general, intact PRD1 particles did not degrade or break upon repeated imaging. On already degraded particles, gradual further deterioration was observed, and particles were also found to detach from the surface. Images were plane fitted when required, using Gwyddion software (; <http://gwyddion.net/>) without the application of noise filtering or sharpening. Nano-indentation measurements were performed at individually selected particles using the 'point-and-shoot' function within the NanoScope software. Briefly, the area of interest was first imaged to localize the virus particle; the 'point-and-shoot' function was then activated and force curves were taken at the particle centre. subsequently, the area was imaged once more to verify successful nano-indentation. The accuracy of localization of the particle centre was found to be limited by piezo drifts and estimated to be within 5 nm. Force *vs.* distance (*F*/*z*) curves were acquired at a constant approach velocity of 200 nm s^--1^. The approach and retract distances were 100 nm, corresponding to a total time of 1 s per complete approach and retract cycle. The maximal load was 4 nN, except for P3-shells, where the maximal load was lowered to 2 nN. *F*/*z* curves were analysed using the NanoScope software. 2.5. Force curve analysis ------------------------- ### 2.5.1. Selection of force curves At maximal loads of 2 to 4 nN, the AFM tip typically reached the underlying support following the indentation and/or fracture of all PRD1-derived particles. We used the *z* distance travelled between the onset of a repulsive force and the closest approach as an indicator for successful indentation at a central particle position. The closest approach typically corresponded to hard-wall contact, though in some cases it was short of hard-wall contact by a few nm as estimated from force curves with hard-wall contact acquired shortly before/after on a nearby mica area and taking advantage of the AFM\'s closed loop *z* scanner. Force curves showing distances of 60 ± 10 nm were retained for further analysis of wt PRD1, Sus1 procapsids, and P3-shells; and distances of 28 ± 5 nm were considered acceptable for DNA-filled vesicles. When imaging vesicles, we found a second class of objects with a height of 12 ± 7 nm and lateral dimensions comparable to the DNA-filled vesicles. Since negative stain EM showed also deformed vesicles in some cases (Fig. S2[†](#fn1){ref-type="fn"}), most likely this second class represents vesicles that lost their DNA and had flattened on the surface. These flattened objects were not further analyzed. To avoid including particles that might have been displaced or changed orientation upon indentation, force curves where force levels dropped and remained below 500 pN over distances of 20 nm and more before hard-wall contact were also discarded from analysis. A representative force curve for each PRD1 particle type with AFM micrographs before and after indentation is shown in Fig. S3,[†](#fn1){ref-type="fn"} and additional force curves illustrating sample to sample variations are shown in Fig. S4.[†](#fn1){ref-type="fn"} ### 2.5.2. Determination of yield point and stiffness After the first contact between the AFM probe and a PRD1 particle at the contact point *z*~c~, the initial monotonous force (compression) was followed by an extended and steep drop (fracture), with subsequent, typically minor, compression and fracture phases (Fig. S4[†](#fn1){ref-type="fn"}). The onset of the first drop, defined as the yield point *z*~y~, is determined by the yield force *F*~y~ = *F*(*z*~y~) and the yield strain *ε*~y~ = (*z*~c~ -- *z*~y~)/*h*, where *h* is the mean particle height. Neglecting the lowest forces (*F* \< 200 pN), which would correspond to a non-linear Hertzian regime of capsid compression,[@cit27] the major part of the first compression phase for wt PRD1, the Sus1 procapsid, and the P3-shell could, in general, be approximated well by a straight line -- with the exception of short stochastic slips that we interpret as micro-fractures (Fig. S5[†](#fn1){ref-type="fn"}). Whilst for hollow-shell particles (Sus1 procapsid and P3-shell), the linear regime can be attributed to elastic shell bending,[@cit27] we focused analysis on this regime also for the full particles (wt PRD1 and vesicle). The particle stiffness *k* was determined from the slope in the initial compression phase, *i.e.*, the slope up to the force at which the first slip or the fracture occurred. In any case, linear fits were not extended beyond 1500 pN (or strains above 10%) to avoid bias by non-linearity at larger compressions. Likewise, the stiffness was not quantified if the first slip occurred below 500 pN to avoid the large uncertainties associated with fitting a line to a small dataset. Stiffness values for vesicles were extracted from linear fits to the compression curves that did not extend beyond 600 pN, but typically up to a maximum of 50% strain, as strains below 15--20% fell within the noise limit of the measurements. ### 2.5.3. Estimation of particle toughness Toughness *T* was defined as the amount of energy *E*~y~ per volume *V* that the PRD1 particles can withstand before breaking. Approximating the virus as a sphere of radius *R*, and with *T* = *E*~y~/*V*, *E*~y~ ≈ *F*~y~(*z*~c~ -- *z*~y~) = *F*~y~*ε*~y~*h* and *V* = 4π/3 *R*^3^ ≈ π/6 *h*^3^, we obtain *T* ≈ 6/π *F*~y~*ε*~y~/*h*^2^. ### 2.5.4. Statistical analysis Origin data analysis and graphing software was used for statistical analysis of results (OriginLab, Northampton, MA). Gaussians were fitted to the histograms in [Fig. 2](#fig2){ref-type="fig"} to extract the means and standard deviations (s.d.). One-way ANOVA tests were performed to determine the statistical significance of the differences of yield force and stiffness across the PRD1-derived particle populations. The stiffness of wt PRD1 against Sus1 procapsid yielded a *P*-value ≤ 0.001 (\*\*), while the stiffness, yield force and yield strain of both PRD1 and Sus1 procapsid against P3-shell showed a *P*-value ≤ 0.0001 (\*\*\*). ![Histograms of various properties of the four viral particle types, reporting mean values and standard deviations for each. *y*-Axis: number of unique particles (75 for wt PRD1 and Sus1 procapsid, 103 for P3-shell and 21 for vesicles). *x*-Axis: property denoted below each column. Specimen heights closely match the particle dimensions previously obtained by averaging techniques, except for the vesicle, which is slightly flattened upon immobilization. Yield force and strain are not shown for vesicles, as these do not have a defined yield point.](c8nr00196k-f2){#fig2} 2.6. Finite-element analyses ---------------------------- To test how the membrane vesicle affects the stiffness and stability in a composite system of a proteinaceous capsid shell with an underneath membrane vesicle, modelling of the mechanical response of PRD1 was performed using a continuum-mechanics finite-element analysis (FEA) with the software ABAQUS 6.14 (ABAQUS, Fremont, CA) (Fig. S6 and S7[†](#fn1){ref-type="fn"}). In this approach, the proteinaceous capsid and the proteo-lipidic vesicle were represented as mechanically isotropic spherical shells, *i.e.*, neglecting the structural details of each shell (see section 3.3). This method can effectively deal with the architectural complexity introduced by the presence of the vesicle whilst the number of adjustable parameters is kept small. 3.. Results and discussion ========================== 3.1. Imaging PRD1 assemblies at the single particle level --------------------------------------------------------- When immobilized, the wt particles oriented with a 3-fold, 2-fold or 5-fold symmetry axis normal to the supporting surface ([Fig. 1c](#fig1){ref-type="fig"}). The preferred orientation (\>67% of the particles) was with a facet down (*i.e.*, a 3-fold axis normal to the surface). The average height was 67.8 ± 2.5 nm (mean ± s.d.) for wt PRD1, 66.9 ± 2.7 nm for the Sus1 procapsid (*n* = 75 each; [Fig. 2a and b](#fig2){ref-type="fig"}, and 62.8 ± 3.5 nm for the P3-shell (*n* = 103; [Fig. 2c](#fig2){ref-type="fig"}), in good agreement with electron-microscopy and X-ray data[@cit7],[@cit28],[@cit29] (Fig. S1b[†](#fn1){ref-type="fn"}). Strikingly, we observed on the Sus1 procapsid a mild circular depression, ∼13 nm in diameter at ∼8% of the visualized vertices (*n* = 103) ([Fig. 1d](#fig1){ref-type="fig"} and S8[†](#fn1){ref-type="fn"}). This percentage, combined with the estimated dimensions, defines at the single-molecule level that this feature is the unique vertex that lacks the external part of the packaging portal.[@cit12] This, however, was not detected on wt PRD1. Indeed, the structural difference in the capsid context between the 'wild type' unique vertex and the remaining 11 vertices is much smaller than that between the unique vertex and the other 11 vertices in the procapsid,[@cit12] and apparently, it is too small to be resolved with our AFM set-up. P3-shells showed holes, ∼25 nm wide, at each vertex ([Fig. 1e](#fig1){ref-type="fig"}) consistent with the missing peripentonal P3 capsomers, spike complexes, and internal vesicles[@cit28],[@cit29] (Fig. S1b[†](#fn1){ref-type="fn"}). The forces needed to be lowered from ∼100 to ∼80 pN to enable imaging of P3-shells indicating that these particles are more sensitive to breakage compared to wt PRD1. By contrast, vesicles displayed a featureless surface and a height of 28.2 ± 4.1 nm ([Fig. 1f](#fig1){ref-type="fig"} and [2d](#fig2){ref-type="fig"}). This height is less than the diameter of DNA-containing vesicles (∼35 nm),[@cit8] indicating that vesicles readily deform when immobilized. 3.2. Stiffness of PRD1 particles -------------------------------- The AFM force *vs.* distance (*F*/*z*) curves (Fig. S3 and S4[†](#fn1){ref-type="fn"}) generated by the nanoindentation testing of individual particles quantified the resistance to small elastic deformation (stiffness, *k*), as well as the force and strain at the point of mechanical failure (yield force, *F*~y~; yield strain, *ε*~y~) ([Fig. 2](#fig2){ref-type="fig"} and [3a--c](#fig3){ref-type="fig"}). ![Comparison of the average mechanical properties across the different PRD1-derived particles. In all panels: black bar, PRD1 wt; pink bar, Sus1 procapsid; blue bar, P3-shell; orange bar, vesicle. (a) Stiffness (*k*); (b) yield force (*F*~y~); (c) yield strain (*ε*~y~); (d) toughness (*T*). All panels report the mean values and standard errors of the mean that were derived from the data shown in [Fig. 2](#fig2){ref-type="fig"} (for the vesicle, calculation of toughness is not possible because there is no defined yield point).](c8nr00196k-f3){#fig3} The *F*/*z* curves typically exhibited a relatively small non-linear regime at the smallest indentation forces (*F* \< 200 pN), which is likely to represent the Hertzian deformation of the capsid shell.[@cit27] This was followed by an extended linear regime, justifying the quantification of elastic properties in terms of the stiffness *k*. For quantitative stiffness analysis, we considered this linear regime for strains up to 10%, which was well below the yield point. For quasi-spherical shells such as the Sus1 procapsid and the P3-shell, this linear regime can be associated with shell bending.[@cit27] Wt PRD1 possessed the greatest stiffness (0.57 ± 0.03 N m^--1^, mean ± s.e.m.), followed by the Sus1 procapsid (0.39 ± 0.02 N m^--1^) and the P3-shell (0.22 ± 0.01 N m^--1^; [Fig. 3a](#fig3){ref-type="fig"}). Most likely, the enhanced resistance of wt PRD1 to elastic deformation arises from the pressure exerted by the DNA.[@cit8],[@cit30] PRD1 genome packaging produces a radial expansion of the internal membrane (*e.g.*, the radius of the outer leaflet increases by ∼6%), which presses the vesicle closer to the capsid.[@cit12],[@cit28],[@cit30] The DNA-filled vesicle displayed the least stiffness (0.022 ± 0.002 N m^--1^; [Fig. 3a](#fig3){ref-type="fig"}), indicating that its direct effect on virion stiffness is marginal but that it contributes to virion stiffness by transmitting pressure from the DNA to the capsid. The volume inside the rigid capsid is reduced upon indentation accentuating the effect of DNA pressure on the stiffness of wt PRD1. In contrast, the soft membrane can stretch upon indentation, thus reducing any effect of DNA pressure on the vesicle stiffness. 3.3. Modelling of PRD1\'s shell elasticities -------------------------------------------- To confirm the above findings on PRD1\'s elastic properties, we confronted the experimental data with continuum-mechanics finite-element computational modelling (see Experimental and Fig. S6[†](#fn1){ref-type="fn"}). In this simulation, the particle was placed between a rigid plane and a rigid indenter ([Fig. 4a](#fig4){ref-type="fig"}). The displacement of the rigid plane was constrained, and the indenter apex was modelled as a sphere of 10-nm radius positioned coaxially with the virus-derived particle in the direction normal to the plane. For indentation, the indenter applied a force in the direction normal to the plane. The contact between all bodies was assumed to be hard in the direction normal to the contact (*i.e.*, interpenetration was not allowed) and frictionless in the tangential direction (*i.e.*, relative displacement and rotation were allowed with no constraint). ![(a) Schematic of the spherical two-shell model (outer protein shell in blue, inner vesicle shell in yellow) for the finite-element modelling; three-quarters of the spheres are shown with the indenter apex represented as a grey sphere with the direction of the applied force as indicated by the black arrow; in the bottom right corner, the Cartesian coordinate system; (b) predicted curves of force *vs.* indentation for a protein shell (with *E* = 0.13 GPa, representing the P3-shell; black dots), a vesicle shell (with *E* = 0.021 GPa, representing the proteo-lipidic vesicle; red dots) and a composite of these protein and vesicle shells (blue dots). In matching colours: lines are linear fits through the origin, and texts the stiffness values corresponding to the slopes. The stiffness values of protein and vesicle shells match the experimental data for P3-shell and vesicle ([Fig. 3a](#fig3){ref-type="fig"}), respectively, confirming the correct choice of Young\'s modulus values; the stiffness of the composite is well approximated by the sum of the stiffness values of the constituent shells and thus only marginally larger than the stiffness of the protein shell alone.](c8nr00196k-f4){#fig4} To extract material properties from the experimental data, we first considered the proteinaceous capsid individually. For the capsid, we estimated an outer radius *R* = 33.2 nm and a thickness *d* = 8 nm from the rotationally averaged electron density maps of the PRD1 virion.[@cit28],[@cit30] By treating the capsid as isotropic and linearly elastic, its properties can be described by two independent parameters: Young\'s modulus *E* and the Poisson ratio *ν*. By neglecting a non-linear regime at very small strains (*ε* \< 3%), the predicted relationship between force and particle indentation *δ* was approximately linear and scaled with the Young\'s modulus *E* for indentations up to 2*d* (*ε* up to 24%; Fig. S6a[†](#fn1){ref-type="fn"}). Our results were rather insensitive to the Poisson ratio (Fig. S7a--c[†](#fn1){ref-type="fn"}), and we thus fixed *ν* = 0.4. These features are consistent with previous computations by others and with the predictions of thin-shell theory,[@cit4],[@cit31],[@cit32] and thus validate the numerical model. The linear relationship between force and indentation is also consistent with our experimental data (Fig. S3b, e, h, and S4a--d[†](#fn1){ref-type="fn"}), where we note that the strain regime of *ε* \< 10% used for the analysis of experimental data lies well within the range over which theory predicts a linear response. This implies that stiffness analysis is far away from any buckling transition.[@cit33] It justifies the use of linear elasticity in our simple theoretical model, and also the use of stiffness *k* = *F*/*δ* to characterize the shell\'s elastic properties. With *F*/*E* ∼ *δ* and *k* = *F*/*δ*, it is also clear that *k* ∼ *E*, and a linear fit to the data in Fig. S6a[†](#fn1){ref-type="fn"} gives *k* ≈ 1.65 nm × *E*. With this equation, we estimate *E* = 0.13 GPa for the P3-shell from the experimentally determined mean stiffness value for this particle (*k* = 0.22 N m^--1^; [Fig. 3a](#fig3){ref-type="fig"}). A recent computational modelling study on a smaller non-membrane-containing virus has shown that capsid proteins can dynamically re-structure upon capsid indentation with appreciable effects on capsid elasticity compared to an idealized homogeneous shell.[@cit34] Our experimental data do not allow deconvoluting these effects. However, the extended linear regime in the *F*/*z* curves observed experimentally for the P3-shell and the Sus1 procapsid (Fig. S4c and d[†](#fn1){ref-type="fn"}) indicates that the bending elasticity of the PRD1 capsid shell remains appropriately described by a Young\'s modulus (where this would effectively include the possible re-structuration effects). The elasticity of the proteolipidic membrane was estimated analogous to that of the proteinaceous capsid, assuming an outer radius identical to the inner radius of the capsid (*R* = 25.2 nm) for direct contact of the two shells, and a membrane thickness *d* = 5.5 nm from a rotationally averaged electron density map.[@cit30] Fig. S6b[†](#fn1){ref-type="fn"} shows the dependence of *F*/*E* on vesicle deformation for these geometrical parameters, from which *k* ≈ 1.07 nm × *E* can be derived. Assuming to a first approximation that the stiffness of the membrane shell is similar to the experimentally accessible value for the genome-containing vesicle (*k* = 0.022 N m^--1^; [Fig. 3a](#fig3){ref-type="fig"}), we can estimate *E* = 0.021 GPa. To predict the elastic behaviour of the composite capsid-membrane system, we modelled a system of two concentric shells with the inner shell adopting the geometry and Young\'s modulus of the membrane and the outer shell adopting the geometry and Young\'s modulus of the P3-shell ([Fig. 4a](#fig4){ref-type="fig"}). The stiffness of this composite system was *k* = 0.24 N m^--1^, that is the presence of the vesicle enhanced the stiffness only marginally, by about 10%, compared to the P3-shell alone. More generally, the stiffness values shown in [Fig. 4b](#fig4){ref-type="fig"} exemplify that the stiffness of the composite (0.24 N m^--1^) is well approximated by the sum of the stiffness values of the constituent shells (0.22 N m^--1^ + 0.02 N m^--1^). The small enhancement in stiffness was virtually independent of the Poisson ratios of both the capsid and membrane (Fig. S7d[†](#fn1){ref-type="fn"}). The above modelling exercise provides reasonable predictions about the trends that can be expected based on the experimental AFM-derived shell elastic mechanical properties. Here, we have operated with the P3-shell as a reference system because experimental data for this single-shell system were readily available. Using the above-identified stiffness relationship, we can now also estimate the Young\'s modulus of the complete capsid shell from the experimentally determined stiffness values of the Sus1 procapsid and the membrane. The closure of 11 of 12 vertices by additional proteins enhances the elasticity of the Sus1 procapsid shell compared to the P3-shell, whilst a further enhancement of the capsid elasticity by the unique vertex -- missing in the Sus1 procapsid -- is likely to be marginal. *k*~capsid~ ≈ *k*~capsid+membrane~ -- *k*~membrane~ ≈ 0.39 N m^--1^ -- 0.02 N m^--1^ = 0.37 N m^--1^ ([Fig. 3a](#fig3){ref-type="fig"}) and *E* ≈ *k*/1.65 nm (Fig. S5a[†](#fn1){ref-type="fn"}) give *E* ≈ 0.22 GPa, a value comparable to that for some non-enveloped and enveloped viral capsids.[@cit35] Indeed, the two-shell modelling confirmed that the stiffness is only marginally affected, by less than 10%, by an internal soft membrane contacting the capsid ([Fig. 4b](#fig4){ref-type="fig"}). The reduced stiffness of the P3-shell (*E* = 0.13 GPa) is likely due to the absence of the stabilizing pentons and peripentonal capsomers. 3.4. Mechanical stability of PRD1 particles ------------------------------------------- The presence of the genome and the ensuing particle stiffening had no appreciable effect on the mechanical stability of the virion: the yield force and yield strain of wt PRD1 (*F*~y~ = 3.0 ± 0.1 nN, *ε*~y~ = 17.5 ± 0.8%; mean ± s.e.m.) and the Sus1 procapsid (*F*~y~ = 2.7 ± 0.1 nN, *ε*~y~ = 18.1 ± 1.4%) were similar ([Fig. 3b and c](#fig3){ref-type="fig"}). This is in contrast to other phages, such as phage *λ*, where the DNA augments both stiffness and mechanical stability.[@cit36] As for the P3-shell, it was much more sensitive to breakage than wt PRD1 or the Sus1 procapsid (*F*~y~ = 0.9 ± 0.1 nN, *ε*~y~ = 12.3 ± 0.7%; [Fig. 3b and c](#fig3){ref-type="fig"}). The mechanical failure of the PRD1 particles upon indentation was frequently accompanied by the loss of capsomers from the capsid shell (Fig. S3a--c,[†](#fn1){ref-type="fn"} insets). In addition, *F*/*z* curves of wt PRD1, the Sus1 procapsid, and the P3-shell revealed slip events coincident with the occurrence of micro-fractures during force loading likely reflecting the local displacements of MCPs (Fig. S5[†](#fn1){ref-type="fn"}). While all three particle populations presented a similar density of micro-fractures (average 1.3 per nN of applied compressive force), wt PRD1 and the procapsid withstood more of these fractures before yielding. Previous studies on binary component viral systems -- genome encapsulated by a protein shell -- have highlighted the role of DNA or RNA in contributing to the capsid stiffness where the mechanical reinforcement is achieved by the genome anchoring the protein shell from the interior.[@cit35] In other cases, such as the herpes simplex virus type 1 (HSV-1) nucleocapsid, the stiffness and yield force remain practically the same whether the particle is fully packaged or devoid of the genome, and stabilizing viral proteins appear to be responsible for this assembly type.[@cit37],[@cit38] In PRD1, the Sus1 procapsid and the mature particle display similar yield forces whereas the relative increase in the stiffness of the wt PRD1 can be attributed to the presence of DNA. The packaging of the genome leads to an expansion of the membrane-vesicle increasing the membrane\'s interactions with the capsid proteins.[@cit12],[@cit28]--[@cit30] 3.5. Toughness analysis of PRD1 and other icosahedral dsDNA viruses ------------------------------------------------------------------- The resistance to material fracture is typically expressed as toughness *T*, here defined as the amount of energy per unit volume that can be absorbed before mechanical failure. The toughness of PRD1, 2.2 × 10^5^ J m^--3^, is relatively high compared to that reported for other icosahedral dsDNA viruses (see [Fig. 3d and 5](#fig3){ref-type="fig"}, and Table S2[†](#fn1){ref-type="fn"}). Thus, PRD1 together with human adenovirus is one of the toughest among all icosahedral dsDNA viruses.[@cit7],[@cit39]--[@cit41] Adenovirus shares a common MCP fold and assembly mechanism with PRD1; however, whilst it lacks a membrane, it possesses a complex set of cementing proteins stabilizing the structure -- about 300 in total (composed of sixty copies of each of the proteins IIIa, V, VI, VIII and IX) instead of the mere 60 copies of the single protein species P30 guiding the assembly in PRD1.[@cit7],[@cit42] Altogether, these comparisons highlight that the layered complex of the capsid and membrane vesicle relieves the genome from a stabilizing role and endows PRD1 with remarkably high mechanical stability. To explore how the PRD1 vesicle and capsid together influence toughness, we compared the toughness of the PRD1-derived particles: the Sus1 procapsid, the P3-shell, and the vesicle. The P3-shell (*T* = 0.54 × 10^5^ J m^--3^) was more susceptible to mechanical failure than the Sus1 procapsid (*T* = 2.1 × 10^5^ J m^--3^; [Fig. 3d](#fig3){ref-type="fig"}). The fact that the P3-shell\'s toughness was ∼4-fold less but its stiffness was only 2-fold less revealed its rather stiff, brittle nature ([Fig. 3a](#fig3){ref-type="fig"}). The P3-shell lattice is held together by the (C-I type and C-II type) interactions established by the GON within each facet and along the facets *via* the MCPs C-termini and by the P30 proteins[@cit7] (Fig. S1a[†](#fn1){ref-type="fn"}). The relative ease of breakage of this lattice might facilitate morphological corrections as the capsomers assemble on the vesicle mould during the procapsid formation. Closing the icosahedral vertices with the peripentonal capsomers and penton proteins (Fig. S1a[†](#fn1){ref-type="fn"}) and plugging the unique vertex with the portal complex produce a stable procapsid that can withstand dsDNA translocation powered by the packaging ATPase P9.[@cit12] More generally, the brittle nature of the capsid is not only manifested in the small yield force of the P3-shell but also in the above-mentioned microfractures. The DNA-filled vesicles, on the other hand, did not show a clear yield point and typically recovered their original shape even after strains exceeding 60%, which indicated that they were ductile and very soft ([Fig. 3a](#fig3){ref-type="fig"}). Thus, comparative analysis with other dsDNA viruses indicates that the toughness of PRD1 is superior to most other dsDNA viruses with comparable capsid organization but lacking the membrane, and is only rivalled by adenovirus -- a non-membrane-containing virus -- which is exceptionally rich in cementing proteins stabilizing the capsid ([Fig. 5](#fig5){ref-type="fig"}). ![PRD1\'s mechanical properties compared to other dsDNA viruses. Key for the viruses and particle types shown in the other panels (in the case of HSV-1 virion, we refer to its nucleocapsid). Comparison across viruses *via* Ashby plots of toughness (*y*-axis in log scale) *vs.* stiffness, yield force and yield strain (*x*-axis), respectively (see the Table S2[†](#fn1){ref-type="fn"} for references).](c8nr00196k-f5){#fig5} 3.6. Composite material model of PRD1 ------------------------------------- Our findings indicate that the capsid is stiff and brittle, whereas the membrane vesicle is ductile and soft. Might the hierarchical combination of these contrasting material properties be responsible for the high toughness of PRD1 particles? Quantifying accurately the contribution of the membrane vesicle to the overall toughness displayed by the PRD1 particle remains a challenge. To our knowledge, no PRD1 intact capsid particles can be biochemically or genetically produced that would allow the AFM probing, and yet the resulting information might be still limited for an exhaustive modelling of the yield behaviour of the full capsid as a brittle material. However, in nature, other macroscopic systems use similar arrangements to create tough materials. One such illustrative example is the coat protecting bird egg, in which a stiff, yet brittle, calcified shell is bonded to a soft and compliant proteinaceous inner skin[@cit43] ([Fig. 6a](#fig6){ref-type="fig"}). ![(a) Multilayered structure of an avian eggshell; (b) cryo-electron density of wt PRD1 with an octant removed displayed in Chimera[@cit45] to show (inset) the layered/composite structure of the virion with the proteinaceous shell in blue, the membrane-vesicle in yellow-lime (OL: outer leaflet; IL: inner leaflet) and with the horizontal black lines marking the distinct layers and the interacting matrix region between the capsid and the membrane. As cartoon representation in red fitted in density the P3 MCPs with N-terminal α-helices interacting with the OL and the P16 transmembrane protein crossing the membrane vesicle. The dsDNA has been removed from within the membrane vesicle for clarity; (c) schematic of a composite sandwich material to which (a) and (b) recapitulate.](c8nr00196k-f6){#fig6} Altogether, these layers constitute a tough composite material that protects the progeny against mechanical stress while carrying out other essential functions. Analogously, the PRD1 capsid and vesicle are bonded to protect the integrity of the virion and its genome ([Fig. 6b](#fig6){ref-type="fig"}). Specifically, the connection between the capsid and membrane vesicle is made of polypeptide stretches: the capsid shell -- composed of 240 copies of interacting trimers of the MCP P3 and glued at the icosahedral edges by the cementing protein P30 -- anchors the membrane through several N-termini of MCPs P3; this connectivity is further augmented by the anchoring N-terminal transmembrane helix of protein P16 located at the base of the peripentonal MCPs P3 [@cit7] (inset in [Fig. 6b](#fig6){ref-type="fig"}). Moreover, it is conceivable that during force loading onto the capsid, these connectors will act as nano-staples increasing the capability of the system of absorbing energy before mechanical failure (an additional energetic cost would be necessary to disrupt protein--membrane interactions[@cit44]). 4.. Conclusions =============== Composites have evolved in nature driven by selection for the efficient use of materials, adaptability, and multi-functionality. Viruses can be seen as composite biological entities where nucleic acids, proteins and lipids assemble to produce functional particles for infection. We propose that, as in a composite sandwich material ([Fig. 6c](#fig6){ref-type="fig"}), an interfacial protein/polypeptide matrix in PRD1 generates a tight connection that mechanically couples the capsid and the membrane ([Fig. 6b](#fig6){ref-type="fig"}). The flexibility of this matrix and possibly also the fluidity of the membrane facilitate the displacement of the two shells relative to each other, and thus assist in maintaining the capsomers in place whilst allowing for the correction of small scale defects in the (re-)assembly process. In summary, we here presented the nanomechanical characterization of a virus that features a membrane inside its capsid. The combination of a stiff, yet brittle, proteinaceous capsid with a soft proteolipidic vesicle in PRD1 facilitates multiple stages of the virus life cycle, including virus assembly, mechanical protection for the extracellular virion, and the vesicle-to-tube transformation during DNA ejection.[@cit13] From a broader perspective, it appears that the evolution of membrane-containing viruses has yielded, at the nanometer scale, composite properties comparable to those known for macroscopic natural materials, where the capsid and vesicle are bonded into a tough composite that protects the integrity of the virus and its genome. Our findings provide both foundational quantitative information and inspiration that can encourage the engineering of tough nanoscale devices and particles capable of protecting fragile cargos. Conflicts of interest ===================== There are no conflicts to declare. Supplementary Material ====================== Supplementary information ###### Click here for additional data file. We thank Sari Korhonen and Helin Veskiväli at the Instruct Centre for Virus and Macromolecular Complex Production (ICVIR; 2009--2017), University of Helsinki, for skilled technical assistance in virus production and purification (the current Biocomplex). We are grateful to the Abrescia Lab\'s members Eva S. Cunha, Diego Charro and Hani Y. Boshra for discussions throughout the study and Isaac Sántos-Pérez for help in virus production and electron microscopy imaging. David I. Stuart at the University of Oxford is also acknowledged for the permission to adapt original images for use in Fig. S1a.[†](#fn1){ref-type="fn"} We also thank MINECO for the Severo Ochoa Excellence Accreditation to the CIC bioGUNE (SEV-2016-0644) and the University of Helsinki and Academy of Finland (grant 1306833) for the support to Biomolecular Complex Purification (Biocomplex), part of Instruct-FI, used in this study. This research was supported by Bruker -- Spain (to S. A. and N. G. A. A.), by the Academy of Finland (Academy Professor funding grants 283072 and 255342 to D. H. B.), by the European Research Council (starting grant FP7-ERC-2012-StG-306435 to R. P. R.), and by the Spanish Ministry of Economy and Competitiveness (MINECO/FEDER; MAT2014-54867-R to R. P. R.; MAT2015-63704-P to G. A. S.; BFU2015-64541-R to N. G. A. A.). [^1]: †Electronic supplementary information (ESI) available. See DOI: [10.1039/c8nr00196k](10.1039/c8nr00196k)
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Increased miniaturization of components, greater packaging density of an integrated circuit die (“IC”), higher performance, and lower cost are ongoing goals of the computer industry. IC package technology continues advances in miniaturization to increase density of integrated circuit or semiconductor components within these packages. The miniaturization of IC packages decreases sizes of products made from these packages in response to continually increasing demands for information and communication products in ever-reduced sizes, thicknesses, and costs, along with ever-increasing performance. These increasing requirements for miniaturization are particularly noteworthy, for example, in portable information and communication devices such as cellular phones, hands-free cellular phone headsets, personal data assistants (“PDA's”), camcorders, notebook computers, and so forth. All of these devices continue to be made smaller and thinner to improve their portability. Accordingly, a large-scale integrated circuit (“LSI”) within an IC package is required to be made smaller and thinner. The LSI package configurations that house and protect the LSI are required to be made smaller and thinner as well. Many conventional packages for integrated circuits, semiconductors or chips are of the type where a semiconductor die is molded into a package with a resin, such as an epoxy molding compound. These packages have a lead frame whose leads are projected from the package body to provide a path for signal transfer between the die and external devices. Other conventional package configurations have contact terminals or pads formed directly on the surface of the package. Such a conventional semiconductor package is fabricated through the following processes: a die-bonding process (mounting the semiconductor die onto the paddle of a lead frame), a wire-bonding process (electrically connecting the semiconductor die on the paddle to inner leads using lead frame wires), a molding process (encapsulating a predetermined portion of the assembly, containing the die, inner leads and lead frame wires, with an epoxy resin to form a package body), and a trimming process (completing each assembly as individual, independent packages). The semiconductor packages thus manufactured are then mounted by matching and soldering the external leads or contact pads of the package to a matching pattern on a circuit board to enable power and signal input/output (“I/O”) operations between the semiconductor devices in the packages and the circuit board. Different challenges arise from increased function integration and miniaturization. For example, a semiconductor product having increased function may be smaller but still require a large number of inputs/outputs (I/O). The size reduction increases the I/O density or decreases the I/O pitch for the integrated circuit die package and its respective integrated circuit die carriers. The ever-increasing I/O density trend presents a myriad of manufacturing problems. Some of these problems reside in the IC die manufacturing realm, such as fine pitch connections and reliability of these connections. Others problems involve mounting these increase I/O density integrated circuit dies on carriers for packaging. Yet other problems reside in the realm of the printed circuit board or the system board that receives the integrated circuit die package having the fine pitch I/O or a large number of I/Os in an ever-shrinking space. Thus, a need still remains for an integrated circuit die package system providing low cost manufacturing, improved yield, and improved reliability. In view of the ever-increasing need to save costs and improve efficiencies, it is more and more critical that answers be found to these problems. Solutions to these problems have been long sought but prior developments have not taught or suggested any solutions and, thus, solutions to these problems have long eluded those skilled in the art.
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Preventing nutritional disorders in athletes: focus on the basics. The prevention of nutritional disorders in athletes is often a controversial topic. The answer centers on the practitioners ability to assess each participant's individual needs, ensuring that basic nutrient requirements are met. The cornerstone to any athlete's nutritional program is to ensure an adequate energy intake correctly proportioned with macronutrients. Inherent to this goal is the understanding that exposure to chronic stress alters energy depots: musculoskeletal structure and immune/inflammatory responses that either facilitate or hinder training based on recovery. Essential to the athlete's health is the understanding that each is a unique individual who will never fit neatly into a predefined, cookbook approach to nutrition. Failure to meet these objectives will only impair recovery. Although quality training and adequate rest is important to training, so too is adequate energy balance. This article focuses on better understanding the benefits of adequate energy balance, further enhanced by a better understanding of macronutrient use.
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Challenges to developing countries after joining WTO: risk assessment of chemicals in food. FAO/WHO encourages member countries to develop national food control measures based on risk assessment in order to assure proper protection level to consumers and facilitate fair trade. This is particularly important for developing countries as WTO members because it is clearly stated in the Sanitary and Phytosanitary Measures (SPS) Agreement that: (a) SPS measures should be based on risk assessment techniques developed by relevant international organizations; and (b) Codex standards which is based on risk assessment are regarded as the international norm in trade dispute settlement. When conducting risk assessment on food chemicals (including additives and contaminants) in developing countries, in most cases it is not necessary to conduct their own hazard characterization because the ADIs or PTWIs of food chemicals developed by international expert groups (e.g. JECFA) are universally applicable and also developing countries do not have the resources to repeat those expensive toxicological studies. On the other hand, it is necessary to conduct exposure assessment in developing countries because exposure to food chemicals varies from country to country. This is not only crucial in setting national standards, but also very important for developing countries to participate in the process of developing Codex standards. In addition to food standard development, risk assessment is also useful in setting up priorities in imported food inspection and evaluating the success of various food safety control measures.
3.1875
3
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The British government has dealt a body blow to hopes of mitigating global warming by capturing greenhouse gases. But is it fatal? An opinion article for NewScientist on carbon capture and storage in the UK by Stuart Haszeldine the world’s first professor of CCS and head of the Scottish Carbon Capture and Storage centre. He provides advice to both the British and the Scottish governments and is a fellow of the Royal Society of Edinburgh, UK. He was awarded the 2011 William Smith medal of the Geological Society of London. After months of speculation, the British government has set back the development of one of the most promising weapons in the war on climate change. The government had a plan to build the world’s first industrial-sized carbon capture and storage (CCS) system on a coal-fired power plant. In CCS, carbon dioxide is removed from power-plant emissions and injected into the microscopic pores of geological storage reservoirs deep below ground. But Chris Huhne, the British secretary of state for energy, has said that the government has failed to reach agreement with its private-sector partners in the project. Electricity producer ScottishPower and its consortium partners National Grid and Shell UK were to have built a system to decarbonise one-sixth of the output at Longannet, the UK’s second-largest coal power plant and at 2.4 gigawatts the third largest in Europe. Now it joins a number of deferred, redesigned or cancelled CCS projects around the world. The UK has become a global leader in all the peripherals that might enable CCS to happen. There are legal greenhouse gas reduction targets, and the European Union’s CCS directive has been transferred into UK law; there is a government office of CCS; there are rules, regulations and permits for storage; and there are even plans (still in draft) to provide premium prices for decarbonised electricity and so encourage commercial funding for CCS power plants. However, all new industries require the first project to be built, and that central piece of the UK jigsaw is still missing. If CCS is to take its place as one of the pillars of UK energy policy – as Huhne has said it will – where do recent events leave a country that likes to provide global leadership on such issues? Plan comes together Longannet would have seen a large new capture plant built. Two million tonnes of pure CO2 gas each year would have been slightly compressed and transported via existing pipelines to St Fergus on the north-east coast of Scotland. Here it would have been compressed into a liquid that would have travelled in existing offshore pipes to Shell’s Goldeneye gas field, where up to 30 million tonnes of CO2 storage has been planned. With this plan, the UK has the world’s most detailed design for a commercial CCS operation. It is technically clear that each part of the CCS chain could work: the storage site is outstanding; the pipeline transport is safe, secure and agreeable to the public; the capture units can be built; they can be operated flexibly; and they can work and to the required environmental and purity standards. There is no doubt that CCS can be built, and that CCS can operate. What went wrong? Money was the problem. The competition to establish the UK’s first CCS scheme has been running since 2007, and the policy and business worlds have moved on since then. ScottishPower is now owned by the Spanish company Iberdrola, which is globally focused on wind and hydro power. There have been three UK prime ministers, a Climate Change Act, threeEnergyActs and three potential mechanisms to fund CCS. It takes corporate stamina to run that marathon. The home straight for Iberdrola was the introduction of electricity market reform in the UK. This has the entirely correct objective of providing long-term certainty in electricity prices, to enable investment in low-carbon technologies. However, only the first part of this reform is currently visible – a new tax on emissions that starts at £15.70 per tonne of CO2 in 2013, rising to £30 per tonne by 2020 and £70 by 2030. However, the plans to charge more for decarbonised electricity and so encourage CCS investments have not yet emerged from the discussion stage. Risk wrangling A second part of the problem lies in the way the UK government finances projects. In a £1 billion endeavour it is important to control costs, which means setting a budget. However, this is difficult if no similar project has been done before, anywhere. ScottishPower submitted detailed cost estimates that said that with good management and good luck the cost could be £1 billion, but with bad management or bad luck it could be £1.52 billion. Who was to carry that £520 million risk? In the view of the Treasury – the UK’s finance ministry – it lies with the developer, and only £1 billion was made available. That is what led to the failure to agree: the company wanted the government to provide a £500 million contingency fund, the government wanted the company to keep to a firm price. There are four points to make. Firstly, the UK is set for another clarification of policy. Gas is now producing about 50 per cent of UK electricity, and with most UK coal generation expected to close before 2022, it is inevitable that much more gas generation will be built. Although cleaner than coal, gas is still a dirty fuel: CCS will still be needed, and proof of its viability is needed well before CO2 reduction targets start to bite in 2020. Europe, not China Secondly, the UK could consider where the true value in CCS lies. This now looks less like exports of hardware to China and more like meeting domestic legal targets for low carbon emissions. It might also allow the UK to generate income by becoming the offshore geological storage destination for CO2 from all of north-west Europe. Such storage needs to be tested soon with real injection, allowing 10 years for the results to emerge. ScottishPower would have achieved that at Longannet. Thirdly, we should use the knowledge gained from Longannet evaluations to make subsequent projects happen faster. Fourthly, the funding for big CCS projects needs to be reconsidered. The premium electricity price for decarbonised power, which is in the pipeline, will encourage commercial investment, but any government that wants to be a leader in CCS will also have to underwrite more of the financial risk that is inevitable in such pioneering projects. In the UK, such factors point to Peterhead gas plant being the next CCS candidate: it would be much cheaper, quicker and easier to develop. After that, there is a strong case for looking to Yorkshire, where the Don Valley coal gasification power plant could send CO2 to offshore oil fields with pipes that can geographically link up with the large Drax coal-fired power plant – which supplies 5 per cent of the UK’s electricity. So CCS may be bruised, but it is not dead. No Plan B has emerged to help mitigate climate change. There is still time for CCS to make a big, unique reduction in global CO2 emission rates. The UK should be part of that. Post navigation Welcome to STRONGOPINIONS.ORG. Here you will find a collection of opinion articles written by scientists and other academic thinkers, contributing to the broad sustainability debate. This includes matters like climate change, biodiversity loss, demographic trends, energy use, resources management and sustainable agriculture. Articles and authors are selected by showing subject-matter expertise as well as refreshing insights..
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Rendering (animal products) Rendering is a process that converts waste animal tissue into stable, usable materials. Rendering can refer to any processing of animal products into more useful materials, or, more narrowly, to the rendering of whole animal fatty tissue into purified fats like lard or tallow. Rendering can be carried out on an industrial, farm, or kitchen scale. The majority of tissue processed comes from slaughterhouses, but also includes restaurant grease and butcher shop trimmings and expired meat from grocery stores. This material can include the fatty tissue, bones, and offal, as well as entire carcasses of animals condemned at slaughterhouses, and those that have died on farms, in transit, etc. The most common animal sources are beef, pork, mutton, and poultry. The rendering process simultaneously dries the material and separates the fat from the bone and protein. A rendering process yields a fat commodity (yellow grease, choice white grease, bleachable fancy tallow, etc.) and a protein meal (meat and bone meal, poultry byproduct meal, etc.). Rendering plants often also handle other materials, such as slaughterhouse blood, feathers and hair, but do so using processes distinct from true rendering. The occupation of renderer has appeared in "dirtiest jobs" lists. Process variations The rendering process varies in a number of ways: Whether the end products are used as human or animal food depends on the quality of input material and the processing methods and equipment. The material may be processed by wet or dry means. In wet processing, either boiling water or steam is added to the material, separating fat into a floating phase. In dry processing, fat is released by dehydrating the raw material. The temperature range used may be high or low. Rendering may be done either in discrete batches or in a continuous process. The processing plant may be operated by an independent company that buys input material from suppliers, or by a packing plant that produces the material in-house. Rendering processes for edible products Edible rendering processes are basically meat processing operations and produce lard or edible tallow for use in food products. Edible rendering is generally carried out in a continuous process at low temperature (less than the boiling point of water). The process usually consists of finely chopping the edible fat materials (generally fat trimmings from meat cuts), heating them with or without added steam, and then carrying out two or more stages of centrifugal separation. The first stage separates the liquid water and fat mixture from the solids. The second stage further separates the fat from the water. The solids may be used in food products, pet foods, etc., depending on the original materials. The separated fat may be used in food products, or if in surplus, may be diverted to soap making operations. Most edible rendering is done by meat packing or processing companies. Rendering processes for inedible products Materials that for aesthetic or sanitary reasons are not suitable for human food are the feedstocks for inedible rendering processes. Much of the inedible raw material is rendered using the "dry" method. This may be a batch or a continuous process in which the material is heated in a steam-jacketed vessel to drive off the moisture and simultaneously release the fat from the fat cells. The material is first ground, then heated to release the fat and drive off the moisture, percolated to drain off the free fat, and then more fat is pressed out of the solids, which at this stage are called "cracklings" or "dry-rendered tankage". The cracklings are further ground to make meat and bone meal. A variation on a dry process involves finely chopping the material, fluidizing it with hot fat, and then evaporating the mixture in one or more evaporator stages. Some inedible rendering is done using a wet process, which is generally a continuous process similar in some ways to that used for edible materials. The material is heated with added steam and then pressed to remove a water-fat mixture that is then separated into fat, water, and fine solids by stages of centrifuging and/or evaporation. The solids from the press are dried and then ground into meat and bone meal. Most independent renderers process only inedible material. History The development of rendering was primarily responsible for the profitable utilization of meat industry by-products, which in turn allowed the development of a massive industrial-scale meat industry that made food more economical for the consumer. Rendering has been carried out for many centuries, primarily for soap and candle making. The earliest rendering was done in a kettle over an open fire. This type of rendering is still done on farms to make lard (pork fat) for food purposes. With the development of steam boilers, it was possible to use steam-jacketed kettles to make a higher grade product, and reduce fire danger. A further development came in the 19th century with the use of steam digesters: a tank used as a pressure cooker where steam was injected into the material being rendered. This process is a wet rendering process called "tanking" and was used for edible and inedible products, although better grades of edible products were made using the open kettle process. After the material is tanked, the free fat is run off, the remaining water ("tank water") run into a separate vat, and the solids removed and dried by pressing and steam-drying in a jacketed vessel. The tank water was either run into a sewer or it was evaporated to make glue or protein concentrate to add to fertilizer. The solids were used for fertilizer. Upton Sinclair wrote The Jungle (1906), an exposé on the Chicago meat processing industry which created public outrage. His work helped the passage of the Pure Food and Drug Act of 1907 which paved the way for the creation of the FDA. The pressure tank made possible the development of the Chicago meat industry in the United States, with its concentration in one geographic area, because it allowed the economic disposal of byproducts which would otherwise overwhelm the environment in that area. At first, small companies that sprang up near the packers did the rendering. Later the packers entered the rendering industry. Gustavus Swift, Nelson Morris, and Lucius Darling were among the early pioneers of the U.S. rendering industry with their personal backing and/or direct participation in the rendering industry. Innovations came rapidly in the 20th century. Some of these were the uses for rendered products, and others were the rendering methods. In the 1920s, a batch dry rendering process was invented; the material was cooked in horizontal steam-jacketed cylinders (similar to the fertilizer dryers of the day). Advantages claimed for the dry process were economy of energy, better protein yield, faster processing, and fewer obnoxious odors. Over the years, the wet "tanking" process was replaced with the dry process. By the end of World War II, most rendering installations used the dry process. In the 1960s, continuous dry processes were introduced, one using a variation of the conventional dry cooker and the other making use of a mincing and evaporation process to dry the material and yield the fat. In the 1980s, high energy costs popularized the various "wet" continuous processes. These processes were more energy efficient and allowed the re-use of process vapours to pre-heat or dry the materials during the process. After WWII, synthetic detergents arrived, which displaced soaps in domestic and industrial washing. In the early 1950s, over half of the inedible fat market vanished. Diversion in these materials into animal feeds soon replaced the lost soap market and eventually became the single largest use for inedible fats. The widespread use of "boxed beef", where the beef was cut into consumer portions at packing plants rather than local butcher shops and markets, meant that fat and meat scraps for renderers stayed at the packing plants and were rendered there by packer renderers, rather than by the independent rendering companies. The rejection of animal fats by diet-conscious consumers led to a surplus of edible fats, and the resultant diversion into soapmaking and oleochemicals, displacing inedible fats and contributing to the market volatility of this commodity. Advantages and disadvantages The rendering industry is one of the oldest recycling industries, and made possible the development of a large food industry. The industry takes what would otherwise be waste materials and makes useful products such as fuels, soaps, rubber, plastics, etc. At the same time, rendering solves what would otherwise be a major disposal problem. As an example, the USA recycles more than 21 million metric tons annually of highly perishable and noxious organic matter. In 2004, the U.S. industry produced over 8 million metric tons of products, of which 1.6 million metric tons were exported. Usually, materials used as raw materials in the rendering process are susceptible to spoilage. However, after rendering, the materials are much more resistant to spoiling. This is due to the application of heat either through cooking in the wet rendering process or the extraction of fluid in the dry rendering process. The fat obtained can be used as low-cost raw material in making grease, animal feed, soap, candles, biodiesel, and as a feed-stock for the chemical industry. Tallow, derived from beef waste, is an important raw material in the steel rolling industry providing the required lubrication when compressing steel sheets. Meat and bones (in a dry, ground state) are converted to meat and bone meal. Health professionals believe that meat and bone meal in animal feed was the main route for the late-20th century spread of bovine spongiform encephalopathy (mad-cow disease, BSE), which is also fatal to human beings. Early in the 21st century, most countries tightened regulations to prevent this. If not for the rendering industry, the cost of waste animal material would be high and would place a significant economic and environmental burden on areas involved in industrial scale slaughtering. This cost would manifest itself through the use of expensive sanitary landfills, incinerators, and other similar waste disposal techniques without yielding profit from opportunity costs. Alternatives to rendering products may not reduce cost. Kitchen rendering Rendering of fats is also carried out on a kitchen scale by chefs and home cooks. In the kitchen, rendering is used to transform butter into clarified butter, suet into tallow, pork fat into lard, and chicken fat into schmaltz. See also Animal slaughter Animal euthanasia Dead Horse Bay Flensing Whale oil References Inline citations General references Lyman, Howard, F. (1998). Mad Cowboy. Simon & Schuster, New York. Render Magazine (April 2005), National Renderer's Association. Meeker, David L. [http://assets.nationalrenderers.org/essential_rendering_book.pdf Essential Rendering: All About The Animal By-Products Industry]. National Renderer's Association. Burnham, Frank. [http://assets.nationalrenderers.org/north_american_rendering_v2.pdf North American Rendering: The Source of Essential High Quality Products]. National Renderer's Association. Clemen, Rudolph (1978). Rendering, The Invisible Industry, Aero Publishers. Young, H.H. (1927). By-Products of the Meat-Packing Industry, University of Chicago Press. Franco, Don and Swanson, Winfield (1996). The Original Recyclers, APPI, FPRF and NRA. Category:Cooking fats Category:Cooking techniques Category:Meat industry Category:Industrial processes
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Female body shape Female body shape or female figure is the cumulative product of her skeletal structure and the quantity and distribution of muscle and fat on the body. There is a wide range of normality of female body shapes. Female figures are typically narrower at the waist than at the bust and hips. The bust, waist, and hips are called inflection points, and the ratios of their circumferences are used to define basic body shapes. Reflecting the wide range of individual beliefs on what is best for physical health and what is preferred aesthetically, as well as disagreements on the social standing and purported 'purpose' of women in society, there is no universally-acknowledged ideal female body shape. Cultural ideals, however, have developed and continue to exert influence over how a woman relates to her own body, as well as how others in her society may perceive and treat her. Physiology Impact of estrogens Estrogens, which are primary female sex hormones, have a significant impact on a female's body shape. They are produced in both men and women, but their levels are significantly higher in women, especially in those of reproductive age. Besides other functions, estrogens promote the development of female secondary sexual characteristics, such as breasts and hips. As a result of estrogens, during puberty, girls develop breasts and their hips widen. Working against estrogen, the presence of testosterone in a pubescent female inhibits breast development and promotes muscle and facial hair development. Estrogen levels also rise significantly during pregnancy. A number of other changes typically occur during pregnancy, including enlargement and increased firmness of the breasts, mainly due to hypertrophy of the mammary gland in response to the hormone prolactin. The size of the nipples may increase noticeably. These changes may continue during breastfeeding. Breasts generally revert to approximately their previous size after pregnancy, although there may be some increased sagging. Breasts can decrease in size at menopause if estrogen levels decline. Fat distribution Estrogens can also affect the female body shape in a number of other ways, including increasing fat stores, accelerating metabolism, reducing muscle mass, and increasing bone formation. Estrogens cause higher levels of fat to be stored in a female body than in a male body. They also affect body fat distribution, causing fat to be stored in the buttocks, thighs, and hips in women, but generally not around their waists, which will remain about the same size as they were before puberty. The hormones produced by the thyroid gland regulate the rate of metabolism, controlling how quickly the body uses energy, and controls how sensitive the body should be to other hormones. Body fat distribution may change from time to time, depending on food habits, activity levels and hormone levels. When women reach menopause and the estrogen produced by ovaries declines, fat migrates from their buttocks, hips and thighs to their waists; later fat is stored at the abdomen. Body fat percentage recommendations are higher for females, as this fat may serve as an energy reserve for pregnancy. Males have less subcutaneous fat in their faces due to the effects of testosterone; testosterone also reduces fat by aiding fast metabolism. The lack of estrogen in males generally results in more fat being deposited around the waist and abdomen (producing an "apple shape"). Muscles Testosterone is a steroid hormone which helps build and maintain muscles with physical activity, such as exercise. The amount of testosterone produced varies from one individual to another, but, on average, an adult female produces around one-tenth of the testosterone of an adult male, but females are more sensitive to the hormone. The muscles most likely to be affected are the pectoral muscles, biceps and the triceps in the arms and quadriceps in the thighs. On the other hand, estrogens reduce muscle mass. Muscle mass changes over time as a result of changes in testosterone and estrogen levels and exercise, besides other factors. Changes to body shape The aging process has an inevitable impact on a person's body shape. A woman's sex hormone levels will affect the fat distribution on her body. According to Dr. Devendra Singh, "Body shape is determined by the nature of body fat distribution that, in turn, is significantly correlated with women's sex hormone profile, risk for disease, and reproductive capability." Concentrations of estrogen will influence where body fat is stored. Before puberty both males and females have a similar waist–hip ratio. At puberty, a girl's sex hormones, mainly estrogen, will promote breast development and a wider pelvis tilted forward for child bearing, and until menopause a woman's estrogen levels will cause her body to store excess fat in the buttocks, hips and thighs, but generally not around her waist, which will remain about the same size as it was before puberty. These factors result in women's waist–hip ratio (WHR) being lower than for males, although males tend to have a greater upper-body to waist-hip ratio (WHR) giving them a V shape look because of their greater muscle mass e.g. they generally have much larger, more muscular and broader shoulders, pectoral muscles, teres major muscles and latissimus dorsi muscles. During and after pregnancy, a woman experiences body shape changes. After menopause, with the reduced production of estrogen by the ovaries, there is a tendency for fat to redistribute from a female's buttocks, hips and thighs to her waist or abdomen. The breasts of girls and women in early stages of development commonly are "high" and rounded, dome- or cone-shaped, and protrude almost horizontally from a female's chest wall. Over time, the sag on breasts tends to increase due to their natural weight, the relaxation of support structures, and aging. Breasts sag if the ligaments become elongated, a natural process that can occur over time and is also influenced by the breast bouncing during physical activity (see Sports bra). Measurements The circumferences of bust, waist, and hips, and the ratios between them, is a widespread method for defining women's body shape in Western cultures. These include terms like "rectangular", "spoon", "inverted triangle", or "hourglass". The measurements are generally described using three numbers to describe the bodily dimensions, or "BWH". The band measurement is usually measured around the women's torso, immediately below her breasts at the inframammary fold, parallel to the floor. The cup size is determined by measuring across the crest of the breast and calculating the difference between that measurement and the band measurement. The waist is measured at the midpoint between the lower margin of the last palpable rib and the top of the iliac crest. The hips are measured at the largest circumference of the hips and buttocks. The waist is typically smaller than the bust and hips, unless there is a high proportion of body fat distributed around it. How much the bust or hips inflect inward, towards the waist, determines a woman's structural shape. The hourglass shape is present in only about 8% of women. Female shapes in the fashion industry Body shapes are often categorised in the fashion industry into one of four elementary geometric shapes, though there are very wide ranges of actual sizes within each shape: Rectangular The waist measurement is less than smaller than the hips and bust measurement. Body fat is distributed predominantly in the abdomen, buttocks, chest, and face. This overall fat distribution creates the typical ruler (straight) shape. Inverted triangle Athletic shaped women have broad(er) shoulders compared with their (narrower) hips. The legs and thighs tend to be slim, while the chest looks larger compared with the rest of the body. Fat is mainly distributed in the chest and face. Spoon The hip measurement is greater than the bust measurement. The distribution of fat varies, with fat tending to deposit first in the buttocks, hips, and thighs. As body fat percentage increases, an increasing proportion of body fat is distributed around the waist and upper abdomen. The women of this body type tend to have a relatively larger rear, thicker thighs, and a small(er) bosom. Hourglass or X shape (triangles opposing, facing in) The hips and bust are almost of equal size with a narrow waist. Body fat distribution tends to be around both the upper body and lower body. This body type enlarges the arms, chest, hips, and rear before other parts, such as the waist and upper abdomen. A study of the shapes of over 6,000 women, carried out by researchers at the North Carolina State University circa 2005, for apparel, found that 46% were rectangular, just over 20% spoon, just under 14% inverted triangle, and 8% hourglass. Another study has found "that the average woman's waistline had expanded by six inches since the 1950s" and that women in 2004 were taller and had bigger busts and hips than those of the 1950s. Several variants of the above coding systems exist: Sheldon: "Somatotype: {Plumper: Endomorph, Muscular: Mesomorph, Slender: Ectomorph}", 1940s Douty's "Body Build Scale: {1,2,3,4,5}", 1968 Bonnie August's "Body I.D. Scale: {A,X,H,V,W,Y,T,O,b,d,i,r}", 1981 Simmons, Istook, & Devarajan "Female Figure Identification Technique (FFIT): {Hourglass, Bottom Hourglass, Top Hourglass, Spoon, Rectangle, Diamond, Oval, Triangle, Inverted Triangle}", 2002 Connell's "Body Shape Assessment Scale: {Hourglass, Pear, Rectangle, Inverted Triangle}", 2006 Rasband: {Ideal, Triangular, Inverted Triangular, Rectangular, Hourglass, Diamond, Tubular, Rounded}, 2006 Lee JY, Istook CL, Nam YJ, "Comparison of body shape between USA and Korean women: {Hourglass, Bottom Hourglass, Top Hourglass, Spoon, Triangle, Inverted Triangle, Rectangle}", 2007. Lee's 2007 paper proposes the following formula be used to identify an individual's body type: Hourglass If (bust − hips) ≤ 1" AND (hips − bust) < 3.6" AND (bust − waist) ≥ 9" OR (hips − waist) ≥ 10" Bottom hourglass If (hips − bust) ≥ 3.6" AND (hips − bust) < 10" AND (hips − waist) ≥ 9" AND (high hip/waist) < 1.193 Top hourglass If (bust − hips) > 1" AND (bust − hips) < 10" AND (bust − waist) ≥ 9" Spoon If (hips − bust) > 2" AND (hips − waist) ≥ 7" AND (high hip/waist) ≥ 1.193 Triangle If (hips − bust) ≥ 3.6" AND (hips − waist) < 9" Inverted triangle If (bust − hips) ≥ 3.6" AND (bust − waist) < 9" Rectangle If (hips − bust) < 3.6" AND (bust − hips) < 3.6" AND (bust − waist) < 9" AND (hips − waist) < 10" In addition a number of national and international clothes sizing standards define body shape coding systems that categorise an individual by the chest to waist and / or hip circumference drop values e.g. Dimensions A woman's dimensions are often expressed by the circumference around the three inflection points. For example, "36–29–38" in imperial units would mean a 36-inch bust, 29-inch waist and 38-inch hips. A woman's bust measure is a combination of her rib cage and breast size. For convenience, a woman's bra measurements are used. For example, though the measurements are not consistently applied, a woman with a bra size of 36B has a rib cage of 36 inches in circumference and a bust measure of 38 inches; a woman with a bra size 34C has a rib cage of 34 inches around, but a smaller bust measure of 37 inches. However, the woman with a 34C breast size will appear "bustier" because of the apparent difference in bust to ribcage ratio. Height will also affect the appearance of the figure. A woman who is 36–24–36 at height will look different from a woman who is 36–24–36 at height. Since the taller woman's figure has greater distance between measuring points, she will likely appear thinner or less curvaceous than her shorter counterpart, again, even though they both have the same BWH ratio. This is because the taller woman is actually thinner as expressed by her height to size ratio. The use of BWH measurements for anything other than garment fitting is thus misleading. BWH is an indicator of fat distribution, not fat percentage. The British Association of Model Agents (AMA) says that female models should be around 34–24–34 (86–61–86 cm) and at least tall. Cultural perceptions According to Camille Paglia, the ideal body type as envisioned by members of society has changed throughout history. She states that Stone Age Venus figurines show the earliest body type preference, dramatic steatopygia; and that the emphasis on protruding belly, breasts, and buttocks is likely a result of both the aesthetic of being well fed and aesthetic of being fertile, traits that were more difficult to achieve at the time. In sculptures from Classical Greece and Ancient Rome the female bodies are more tubular and regularly proportioned. There is essentially no emphasis given to any particular body part, not the breasts, buttocks, or belly. Moving forward there is more evidence that fashion somewhat dictated what people believed were the proper female body proportions. This is the case because the body is primarily seen through clothing, which always changes the way the underlying structures are conceived. The first representations of truly fashionable women appear in the 14th century. Between the 14th and 16th centuries in northern Europe, bulging bellies were again desirable, however the stature of the rest of the figure was generally thin. This is most easily visible in paintings of nudes from the time. When looking at clothed images, the belly is often visible through a mass of otherwise concealing, billowing, loose robes. Since the stomach was the only visible anatomical feature, it became exaggerated in nude depictions while the rest of the body remained minimal. In southern Europe, around the time of the renaissance, this was also true. Though the classical aesthetic was being revived and very closely studied, the art produced in the time period was influenced by both factors. This resulted in a beauty standard that reconciled the two aesthetics by using classically proportioned figures who had non-classical amounts of flesh and soft, padded skin. In the nude paintings of the 17th century, such as those by Rubens, the naked women appear quite fat. Upon closer inspection however, most of the women have fairly normal statures, Rubens has simply painted their flesh with rolls and ripples that otherwise would not be there. This may be a reflection of the female style of the day: a long, cylindrical, corseted gown with rippling satin accents. Thus Rubens' women have a tubular body with rippling embellishments. While the corset continued to be fashionable into the 18th century, it shortened, became more conical, and consequently began to emphasize the waist. It also lifted and separated the breasts as opposed to the 17th century corsets which compressed and minimized the breasts. Consequently, depictions of nude women in the 18th century tend to have a very narrow waist and high, distinct breasts, almost as if they were wearing an invisible corset. La maja desnuda is a clear example of this aesthetic. The 19th century maintained the general figure of the 18th century. Examples can be seen in the works of many contemporary artists, both academic artists, such as Cabanel, Ingres, and Bouguereau, and Impressionists, such as Degas, Renoir, and Toulouse-Lautrec. As the 20th century began, the rise of athletics resulted in a drastic slimming of the female figure. This culminated in the 1920s flapper look, which has informed modern fashion ever since. The last 100 years envelop the time period in which that overall body type has been seen as attractive, though there have been small changes within the period as well. The 1920s was the time in which the overall silhouette of the ideal body slimmed down. There was dramatic flattening of the entire body resulting in a more youthful aesthetic. As the century progressed, the ideal size of both the breasts and buttocks increased. From the 1950s to 1960 that trend continued with the interesting twist of cone shaped breasts as a result of the popularity of the bullet bra. In the 1960s, the invention of the miniskirt as well as the increased acceptability of pants for women, prompted the idealization of the long leg that has lasted to this day. Following the invention of the push-up bra in the 1970s the ideal breast has been a rounded, fuller, and larger breast. In the past 20 years the average American bra size has increased from 34B to 34DD, although this may be due to the increase in obesity within the United States in recent years. Additionally, the ideal figure has favored an ever-lower waist-hip ratio, especially with the advent and progression of digital editing software such as Adobe Photoshop. Social and health issues Each society develops a general perception of what an ideal female body shape would be like. These ideals are generally reflected in the art and literature produced by or for a society, as well as in popular media such as films and magazines. The ideal or preferred female body size and shape has varied over time and continues to vary among cultures; but a preference for a small waist has remained fairly constant throughout history. A low waist-hip ratio has often been seen as a sign of good health and reproductive potential. A low waist–hip ratio has also often been regarded as an indicator of attractiveness of a woman, but recent research suggests that attractiveness is more correlated to body mass index than waist–hip ratio, contrary to previous belief. According to Dr. Devendra Singh of the University of Texas, who studied the representations of women, historically found there was a trend for slightly overweight women in the 17th and 18th centuries, as typified by the paintings of Rubens, but that in general there has been a preference for a slimmer waist in Western culture. He notes that "The finding that the writers describe a small waist as beautiful suggests instead that this body part – a known marker of health and fertility – is a core feature of feminine beauty that transcends ethnic differences and cultures." New research suggests that apple-shaped women have the highest risk of developing heart disease, while hourglass-shaped women have the lowest. Diabetes professionals advise that a waist measurement for a woman of over increases the risk of heart disease, but that ethnic background also plays a factor. This is because body fat buildup around the waist (the apple shape) poses a higher health risk than a fat buildup at the hips (the pear shape). Waist–hip ratio Compared to males, females generally have relatively narrow waists and large buttocks, and this along with wide hips make for a wider hip section and a lower waist–hip ratio. Research shows that a waist–hip ratio (WHR) for a female very strongly correlates to the perception of attractiveness. Women with a 0.7 WHR (waist circumference that is 70% of the hip circumference) are rated more attractive by men in various cultures. Such diverse beauty icons as Marilyn Monroe, Sophia Loren and the Venus de Milo all have ratios around 0.7. In other cultures, preferences vary, ranging from 0.6 in China, to 0.8 or 0.9 in parts of South America and Africa, and divergent preferences based on ethnicity, rather than nationality, have also been noted. Many studies indicate that WHR correlates with female fertility, leading some to speculate that its use as a sexual selection cue by men has an evolutionary basis. However it is also suggested that the evident relationships between WHR-influencing hormones and survival-relevant traits such as competitiveness and stress tolerance may give a preference for higher waist-hip-ratios its own evolutionary benefit. That, in turn, may account for the cross-cultural variation observed in actual average waist-hip-ratios and culturally preferred waist-to-hip ratios for women. WHR has been found to be a more efficient predictor of mortality in older people than waist circumference or body mass index (BMI). Bodies as identity Over the past several hundred years, there has been a shift towards viewing the body as part of one's identity – not in a purely physical way, but as a means of deeper self-expression. David Gauntlett, in his 2008 book, recognizes the importance of malleability in physical identity, stating, "the body is the outer expression of our self, to be improved and worked upon". One of the more key factors in creating the desire for a particular body shape – most notably for females – is the media, which has promoted a number of so-called "ideal" body shapes. Fashionable figures are often unattainable for the majority of the population, and their popularity tends to be short-lived due to their arbitrary nature. During the 1950s, the fashion model and celebrity were two separate entities, allowing the body image of the time to be shaped more by television and film rather than high fashion advertisements. While the fashion model of the 1950s, such as Jean Patchett and Dovima, were very thin, the ideal image of beauty was still a larger one. As the fashion houses in the early 1950s still catered to a specific, elite clientele, the image of the fashion model at that time was not as sought after or looked up to as was the image of the celebrity. While the models that graced the covers of Vogue Magazine and Harper's Bazaar in the 1950s were in line with the thin ideal of the day, the most prominent female icon was Marilyn Monroe. Monroe, who was more curvaceous, fell on the opposite end of the feminine ideal spectrum in comparison to high fashion models. Regardless of their sizes, however, both fashion of the time and depictions of Monroe emphasize a smaller waist and fuller bottom half. The late 1950s, however, brought about the rise of ready-to-wear fashion, which implemented a standardized sizing system for all mass-produced clothing. While fashion houses, such as Dior and Chanel, remained true to their couture, tailor-made garments, the rise of these rapidly-produced, standardized garments led to a shift in location from Europe to America as the epicenter of fashion. Along with that shift came the standardization of sizes, in which garments weren't made to fit the body anymore, but instead the body must be altered to fit the garment. During the 1960s, the popularity of the model Twiggy meant that women favoured a thinner body, with long, slender limbs. This was a drastic change from the former decade's ideal, which saw curvier icons, such as Marilyn Monroe, to be considered the epitome of beautiful. These shifts in what was seen to be the "fashionable body" at the time followed no logical pattern, and the changes occurred so quickly that one shape was never in vogue for more than a decade. As is the case with fashion itself in the post-modern world, the premise of the ever-evolving "ideal" shape relies on the fact that it will soon become obsolete, and thus must continue changing to prevent itself from becoming uninteresting. An early example of the body used as an identity marker occurred in the Victorian era, when women wore corsets to help themselves attain the body they wished to possess. Having a tiny waist was a sign of social status, as the wealthier women could afford to dress more extravagantly and sport items such as corsets to increase their physical attractiveness. By the 1920s, the cultural ideal had changed significantly as a result of the suffrage movement, and "the fashion was for cropped hair, flat (bound) breasts and a slim androgynous shape". More recently, magazines and other popular media have been criticized for promoting an unrealistic trend of thinness. David Gauntlett states that the media's "repetitive celebration of a beauty 'ideal' which most women will not be able to match … will eat up readers' time and money—and perhaps good health—if they try". Additionally, the impact that this has on women and their self-esteem is often a very negative one, and resulted in the diet industry taking off in the 1960s – something that would not have occurred "had bodily appearance not been so closely associated with identity for women". Melissa Oldman states, "Nowhere is the thin female ideal more evident than in popular media." The importance of "the body as a work zone", as Myra MacDonald asserts, further perpetuates the link between fashion and identity, with the body being used as a means of creating a visible and unavoidable image for oneself. The tools with which to create the final copy of such a project range from the extreme—plastic surgery—to the more tame, such as diet and exercise. Alteration of body shape A study at Brigham Young University using MRI technology suggested that women experience more anxiety about weight gain than do men, while aggregated research has been used to claim that images of thin women in popular media may induce psychological stress. A study of 52 older adults found that females may think more about their body shape and endorse thinner figures than men even into old age. Various strategies are sometimes employed to temporarily or permanently alter the shape of a body. The most common include dieting and exercise. At times artificial devices are used or surgery is employed. Breast size can be artificially increased or decreased. Falsies, breast prostheses or padded bras may be used to increase the apparent size of a woman's breasts, while minimiser bras may be used to reduce the apparent size. Breasts can be surgically enlarged using breast implants or reduced by the systematic removal of parts of the breasts. Hormonal breast enhancement may be another option. Historically, boned corsets have been used to reduce waist sizes. The corset reached its climax during the Victorian era. In twentieth century these corsets were mostly replaced with more flexible/comfortable foundation garments. Where corsets are used for waist reduction, it may be temporary reduction by occasional use or permanent reduction by people who are often referred to as tightlacers. Liposuction and liposculpture are common surgical methods for reducing the waist line. Padded control briefs or hip and buttock padding may be used to increase the apparent size of hips and buttocks. Buttock augmentation surgery may be used to increase the size of hips and buttocks to make them look more rounded. Social experiments on the ideal woman's body Two social experiments were performed in 2012, which provided information on a female's ideal body and argued that the ideal body is an unattainable social construct meant to keep women striving to please men's sexual desires. The first experiment, performed by researcher Lon Kilgore, involved measuring multiple people and comparing those measurements to Leonardo da Vinci's representation of the ideal human body, The Vitruvian Man. Kilgore used the conclusions of this experiment to prove that there is no such ideal body for females because the human body is ever changing to adapt to its environment. In the second experiment, researchers Kara Crossley, Piers Cornelissen and Martin Tovée asked men and women to depict an attractive female body and the majority of them had the same diagram. Critical writer Kovie Biakolo uses this to state that society has embedded into us this idea that the ideal woman looks a certain way. Created in 1490, the Vitruvian Man is famously known to be the portrayal of the perfect human, depicting all the perfect proportions and measurements between limbs and features. Because it is so perfect, comparing a person, male or female, to it has been "one of the most familiar and easiest methods of determining if an individual deviates from 'normal' anthropometry." However, Kilgore proves that the majority of men and women do not fit this image. In the experiment, Kilgore measured multiple body parts of nine male subjects and six female subjects, such as height, wingspan, hip width, elbow to fingertip, torso, and legs, and compared those measurements to the measurements of Da Vinci's drawing. The results of the measurements and comparisons demonstrated that "not a single subject in this study possessed the dimensional relationships put forth by da Vinci." Even single measurements of individual limbs of these subjects do not match the figure, proving that the ideal human, The Vitruvian Man, might not be ideal at all. Kilgore explains this anomaly through evolution; he states that the human body never might have been exactly identical to the Vitruvian Man because the human body is always changing to adapt its environment. "In the more than five centuries since, human height has changed." In fact, when Da Vinci was drawing this figure in the 15th century, the average height of men of European ancestry was 5'6"–5'8"; however the average male height today is 5'9"–5'11". Kilgore ends his experiment stating that the Vitruvian Man does not accurately describe the modern male or female. In another social experiment, researchers Kara Crossley, Piers L. Cornelissen, and Martin Tovée explore what an attractive body is, asking multiple men and women to draw their ideal bodies using a virtual program in which they would increase or decrease the sizes of specific body parts. After looking at the depictions of their participants, the researchers came to a conclusion that almost all had depicted similar ideal bodies. The women who participated in this experiment drew their ideal bodies with enlarged busts and narrowed the rest of their bodies, resulting in the conclusion that the representation of ideal female body size and shape was narrowed hips, waist, lower torso, and an enlarged bust. The male participants also depicted their ideal partner with the same image. The researchers state, "For both sexes, the primary predictor of female beauty is a relatively low BMI combined with a relatively curvaceous body." See also Female physical attractiveness Chinese ideals of female beauty Glossary of shapes with metaphorical names Human variability List of artists focused on the female form Sex differences in humans Somatotype and constitutional psychology Thigh gap References Cited sources External links Art and love in Renaissance Italy, Issued in connection with an exhibition held Nov 2008-Feb 2009, Metropolitan Museum of Art, New York (see Belle: Picturing Beautiful Women; pages 246-254) Category:Body shape Category:Female beauty Category:Feminism and health Category:Human body Category:Physical attractiveness
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Steel making is considered a batch process. A unit of steel is melted or made with oxygen in a primary steelmaking vessel. The steel is then transferred to a ladle where it is alloyed and refined. Then the steel is transferred to a distribution vessel called a tundish from which it is distributed to one or more molds for solidification. In each of the batch vessels, a slag is present on the steel, comprised of liquid and solid oxides. The properties of the slag are quite different in each batch operation and it is not desirable to allow the transfer of the slag from one vessel to the next in the production sequence. Slag from the primary steelmaking vessel should not be carried into the ladle, slag formed in the ladle should not be carried into the tundish, and slag from the tundish should not be carried into the molds. At the same time, it is desirable to maximize the yield of metal during transfer operations. Ideally, all the steel and none of the slag should be transferred from one batch operation to the next. Practically, this is not possible since slag and steel tend to form an emulsion or mixture, particularly near the end of a transfer operation. In that case, either some steel must be left untransferred, or some slag must be transferred to the next operation. An object of the present invention is to provide the operator with a tool that will minimize the duration of two phase flow, and to help him to choose by grade the optimum condition for steel retention and slag transfer. It is known that the degree of mixing of slag and steel during a transfer operation increases with the rate of steel flow. At high flow rates, a vortex may develop well before the end of the transfer operation. In that case, steel and slag may flow together for some time, causing an unacceptable amount of slag transfer. It is the object of steel transfer operations to maintain flow that prevent the mixing and co-transfer of steel and slag. An object of the present invention is to indicate the onset of a vortex and to cause a change in the transfer operation to dissipate the vortex, either automatically or by informing the operator of a recommended course of action. In the prevention of slag transfer from one vessel to the next, detection of slag flow is important. In many cases, the detection of slag flow is visual and after the fact. For example, in the tapping of steel from an oxygen steel making vessel, the operator will watch the tap stream and the surface of steel in the ladle for indications of slag flow. A significant amount of slag flow causes the stream to brighten and flare due to the higher emissivity and lower surface tension of slag in relation to steel. Also, the lower density of slag causes it to flow across the surface of the steel in the ladle whereas the steel stream penetrates the surface. These indications cause the operator to stop the transfer operation to prevent the further flow of slag into the ladle, but this is usually after significant slag volume has transferred from the steel making vessel into the ladle. The operators vary in level of skill, experience, and attention to detail, causing the amount of slag carry-over to be quite variable from heat to heat. It is therefore desirable to have an operator independent system that can detect the onset of slag flow during the furnace tapping sequence and cause the modification or end of the tapping sequence to minimize the inflow of slag to the ladle. In another example, when teeming steel from the ladle to the tundish, the operator may watch the pour box area of the tundish for signs of slag flow, such as a brightening of the slag surface around the pouring tube, or a welling up of slag around the pouring tube. Upon seeing these signs, the operator will cause the end of the teeming operation to prevent further flow of slag. Once again, significant slag flow from ladle to tundish may have occurred by that time. Several aids have been developed to detect slag flow from the ladle. One is based on the difference in conductivity between slag and steel and a resistance is continuously measured between two contact points within the nozzle. This method cannot detect vortexing which often precedes slag flow. Also this method fails if the steel fails to contact one of the probes. Additionally, this method fails if the slag flow is in the center of the stream, allowing the steel to contact both probes and the slag to go undetected. U.S. Pat. No. 4,140,300 of Gruner et al teaches a method of slag detection that monitors the radiation intensity of the stream of steel flowing through a discharge tube. A lateral side duct is inserted in the ladle shroud, or discharge tube, through which the steel stream can be observed. A change in radiation intensity signals the onset of slag flow. This method is intrusive and requires side duct modification for each shroud, so it has not found acceptance. Additionally, slag flow through the center of the steel stream would go undetected. Another method of slag detection relies on an indirect method of conductivity measurement using a magnetic field. An electromagnetic coil is placed around the flowing stream of steel. When slag begins to flow, the field properties are changed by the lower conductivity of the stream. The percentage of high conductivity to low conductivity stream area is set at a predetermined rate; and, when this falls below a given threshold, then an alarm signals the operator to shut the ladle stream. Alternatively, the ladle stream can be caused to automatically shut off when the given threshold value is reached. A disadvantage of this method is that vortical flow is not detected. Slag may form only a small percentage of the area of a vortexing stream, and this may not be enough to trigger the alarm to shut the ladle. A further disadvantage of this method is that the electromagnetic coils must be embedded into the refractory bottom of each ladle. These coils require periodic replacement and are a costly maintenance item. Replacement of a damaged coil is usually done when a ladle—is scheduled to be relined with new refractory. Until that time, a ladle may go without slag detection ability for several batches of steel. Yet another method of slag detection relies on the operator's ability to detect a difference in the vibration of a ladle shroud as slag flow begins. Steel has about twice the density of slag, and it causes the ladle shroud to vibrate significantly as it flows from the ladle into the tundish. This vibration tends to increase in strength during vortexing and decrease in strength during slag flow. Thus, a skilled operator can place a hand on the ladle shroud manipulator ann and sense the vibration during the latter part of a ladle pouring operation. The vibration will abruptly diminish as slag begins to flow through the shroud, at which time the operator causes the temlination of the ladle draining operation. A vortex is more difficult to detect by hand, but a skilled operator may also sometimes detect the onset of vortexing flow and may cause the temlination of the ladle draining operation at that point. While this method of slag detection is somewhat effective, it relies greatly on the skill and attentiveness of the operator and is thus inconsistent. Also, the operator does not have the ability to discern the various vibration frequencies associated with operations and activities around the casting machine. Some of these may influence his ability to accurately detect slag. In addition, the operator is influenced by his knowledge of approximate weight of steel left in the ladle. His level of sensitivity in slag detection may be low if he perceives that a significant amount of steel remains, and he may miss the early onset of slag. Conversely, his level of sensitivity may be heightened if he perceives that the ladle is almost empty, and he may terminate the pouring operation leaving a significant amount of steel in the ladle. Instrumentation of the above method of vibration slag detection has been reported in the technical literature in papers from the BHP and NKK steel companies and in the patent literature. In each reported case, an accelerometer was used as a vibration transducer to continuously measure the vibration of the ladle shroud, the shroud manipulator arm or the tundish. In Japanese patent document 58-13455 (January, 1983), there is disclosed monitored vibration of the tundish during steel teeming. The amplified and filtered signal was monitored for a sudden increase and then drop in the amplitude, which signified the onset of slag flow and caused the steel teeming operation to be terminated. The sensitivity of the instrument was increased by also monitoring the rate of change of vibration amplitude with time. K. Yamamoto (Japan 58-13464, January 1983) teaches monitoring the vibration of the ladle shroud to determine the onset of slag flow and automatically terminate teeming. As is the case with the tundish, the shroud vibration amplitude increases with vortexing and decreases with slag flow. In another patent document (Japan Kokai 60-148652, August 1985), there is taught the use of a microphone to monitor the sound of steel flowing through the shroud. The onset of slag flow is marked by a decrease in the sound amplitude. One skilled in the art will realize that sound is, in fact, vibration and the concept is the same as that described in the previously mentioned prior art. The transducer to measure sound may be a piezoelectric accelerometer, a microphone, a Doppler laser device, or any other means that can quantify vibration intensity as a function of time. BHP Steel in Australia reported using analog signal conditioning to filter out low frequency noise associated with crane movements and other background vibrations. The signal to noise ratio was also improved with analog signal conditioning. They measured vibration amplitude and output the signal using an analog meter. The onset of slag due to vortexing was noted by a marked increase in vibration amplitude. The signal dropped off dramatically after slag flowed through the nozzle. The system sounded a threshold alarm when vortexing reached a critical level, but the operators actually learned to read the analog output and take action based on the vibration pattern observed just before the alarm. The system was reported to be better than visual slag detection or manual vibration detection. It also required less maintenance than electromagnetic methods and was considerably less expensive. However, several disadvantages were noted. Firstly, the flow control slide gate had to be set to a low flow level near the end of a transfer operation which caused reduced metal level in the tundish. Secondly, the slide gate could not be moved after it was set in detection mode. Finally, in conditions where a vortex did not form prior to slag flow, the operator reaction was too slow in closing the teeming stream and significant slag flow into the tundish could occur. U.S. Pat. No. 5,042,700 teaches the use of a piezoelectric accelerometer to monitor the vibration of the ladle shroud that is caused by steel flowing through it. It is disclosed that vortexing flow causes an increase in vibration amplitude and that the onset of slag flow causes a decrease in vibration amplitude. The vibration signal is continuously compared to a desired signal and action is taken when the vortexing or slag is indicated by the deviation from the desired signal. Additionally, Ardell teaches that a gradual decrease in vibration amplitude over time without adjustment of any flow control device indicates a blockage of the flow channel, such as might occur with the accretion of aluminum oxide particles within the nozzle. The inventors then address the means to clear such a blockage, such as by a burst of argon through the shroud. In U.S. Pat. No. 5,633,462, it is disclosed that a background vibration signature should be recorded as a comparative signal against which a real time signal is continuously compared. When the real time signal deviates significantly from the background signal, the teeming is caused to stop either by feedback to the flow control device or by alarming the operator. In fact, real time monitoring of vibration, as taught by the prior art, is a continuous comparison of a new amplitude signal to a previous amplitude signal. It is an object of this invention to provide an improved process for detecting slag.
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LEDs are typically mounted on a submount wafer that is later diced to separate out the individual LEDs/submounts. Each submount portion of the wafer has top electrodes that are bonded to electrodes on the LED, such as by ultrasonic bonding. An underfill material, such as epoxy or silicone, is then injected under the LED to provide mechanical support and protect the LED from contaminants. Any underfill material substantially outside of the LED footprint (e.g., outside of 20 microns) is removed so that the submount surface is clean. One reason to remove the underfill material that extends beyond the LED die footprint is that, if the underfill is epoxy (starts off yellow) and is exposed to UV light, the epoxy turns black and absorbs light. The submount also has a set of more robust electrodes, electrically connected by a metal pattern to the LED electrodes, that are typically bonded to a printed circuit board (after the submount wafer is diced) using conventional solder reflow or other means. It is known to provide reflective metal electrodes on the bottom surface of the LEDs so that light emitted downward by the LED active layer is reflected upward rather than being absorbed by the submount. Some of the LED's emitted light also impinges on the submount surface surrounding the LED die footprint. To reflect that light, it is known to deposit a reflective metal ring around the LED, such as silver or aluminum. Forming a metal reflector takes additional steps, and the metal must be insulated from the top metal pattern on the submount. What is needed is a better way to reflect light upwards from the surface of a submount or other LED mounting surface.
3.203125
3
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Out-of-the-box innovation Every day, classrooms around the world demonstrate the powerful sense of collaboration and hands-on learning that Dash, Dot, and Cue inspire in students. Wonder Workshop’s comprehensive solution provides educators with a concrete way to teach an abstract concept–coding; it is the new literacy. Fall in love with the robots’ beloved personalities and with Wonder Workshop’s turnkey resources. A suite of possibilities Everything you need to teach coding through robotics in your classroom. "Wonder Workshops engaging approach to coding and robotics helps my students develop the fundamental skills of collaboration, problem-solving, and persistence through engaging, hands-on activities that enhance lessons in all subjects." TIFFANY HOGG First-grade teacher, Pennsylvania SCHOOL-WIDE "We are doing students a disservice if we teach today the same way as we taught yesterday. Robotics is a great way for students to exercise their critical thinking skills through programming, and watch it come alive through robots." CARRIE WILLIS Technology Director, California DISTRICT-LEVEL "Wonder Workshop’s approach to teaching coding and robotics allows my students to build and develop computer science skills, while also learning the fundamental skills of critical thinking, problem-solving, collaboration, and creative storytelling." KENT STEEN, Ph.D. Curriculum Specialist, Nebraska IN THE CLASSROOM SCHOOL-WIDE DISTRICT-LEVEL No coding experience necessary Wonder Workshop’s comprehensive curricular resources enable teachers to help students practice computational thinking and develop 21st-century skills with Dash, Dot, and Cue robots. Our lesson plans are designed to meet CSTA, ISTE-S, and Common Core State Standards, and are aligned to Code.org’s Computer Science Fundamentals courses and Computer Science Discovery series. Learn to Code Curriculum Designed for K-5 teachers and students, these step-by-step lesson plans cover six fundamental coding concepts and engage kids in hands-on activities and project-based assessments. Applied Robotics Curriculum Steeped in design thinking, the three project-based units offer students choice and voice as they advance to the next level of coding and robotics. Activities Library Discover turnkey activities and lesson plans that can be applied across core subject areas. Search by subject, grade level, and robot/accessory to find the right cross-curricular content for your students’ needs. Training on demand Coding is the new team sport Ignite curiosity and inspire confidence in students ages 6-14 by participating in our annual Wonder League Robotics Competition (WLRC). Teams from around the world compete virtually (and for free) towards three $5,000 STEM grant grand prizes. Press & Media 지원 Get the apps Join the Mailing List Sign up today and get the latest news, product updates, and exclusive newsletter-only offers. Please enter a valid email address. This email address is already subscribed. Thank you! Please check your inbox to complete your subscription. Let's Connect Apple, the Apple logo, and iPad are trademarks of Apple Inc., registered in the U.S. and other countries. App Store is a service mark of Apple Inc. JAVASCRIPT is a registered trademark of Oracle and/or its affiliates. Other names may be trademarks of their respective owners. Wonder Workshop, Inc. is not associated with Oracle and Oracle does not sponsor or endorse Wonder Workshop, Inc., its products or services. This website stores cookies on your computer. These cookies are used to improve your website experience and provide more customized services to you. To find out more about the cookies we use, see our privacy policy. To accept cookies from this site, please click the accept button.
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Researchers have shown that they can create entirely new strains of infectious proteins known as prions in the laboratory by simply mixing infectious prions from one species with the normal prion proteins of another species. The findings are reported in the September 5th issue of the journal Cell, a Cell Press publication. Prion diseases, also known as transmissible spongiform encephalopathies (TSEs), are infectious neurodegenerative diseases affecting the brain of several species of mammals including humans. Creutzfeldt-Jakob disease (CJD) is the most common prion disease in humans, along with scrapie in sheep, bovine spongiform encephalopathy (BSE, aka mad cow) in cattle, and chronic wasting disease (CWD) in deer and other cervids. Unlike conventional infectious microorganisms, the infectious agent in the case of prion diseases consists exclusively of a misfolded form of the prion protein, earlier studies showed. The researchers now find that prion strains produced by combining normal hamster proteins with infectious mouse proteins can infect hamsters and vice versa. Although they are both rodents, prions from one of the two species normally don’t readily infect the other, a common phenomenon amongst prions known as a species barrier, the researchers explained. The novel prions they produced not only look different, but they also produce symptoms in the animals that differ from any known strain found in nature, they report. ” We are forcing the system by putting everything together, but this suggests that the variety of possible prions is really very large,” said Claudio Soto of the University of Texas Medical Branch. “We shouldn’t be surprised if new barriers are crossed and new prions arise. There is the potential for a large variety of new infectious prions—some of which may have dramatic effects.” “The infectous agent is nothing like what we’re used to,” Soto said. “It’s just a protein with a different shape from the normal protein we all have.” Those misfolded and misshapen proteins can spread by causing normal protein to change their shape. Those aberrant forms band together, forming fibrils. Soto’s team recently reported the generation of infectious prions by amplification of prion misfolding in the test tube. In those experiments, they used a technology called protein misfolding cyclic amplification (PMCA) that mimics some of the fundamental steps involved in the replication of infectious prions in living animals, but at an accelerated rate. The method involves placing small quantities of infectious prions with large quantities of the normal protein from the same species together, allowing the infectious form to imprint on the normal form and thereby replicate itself. Now, they show that the same method can generate new strains when infectious prions from one species are mixed with normal prion proteins from another species. The finding provides conclusive evidence that the imprinting of disease-causing prions on normal forms can overcome species barriers, and doesn’t require any other infectious agent. This new insight has profound implications for public health, according to the researchers. ” One of the scariest medical problems of the last decades has been the emergence of a new and fatal human prion disease–variant CJD–originated by cross-species transmission of BSE from cattle,” the researchers said. BSE has also spread to other animals, including exotic cats, other primates and domestic cats, after they ate feed derived from diseased cows. The new method might provide insight into the risk that other prion diseases could spread from one species to another, Soto said. For instance, scientists don’t know whether chronic wasting disease, a condition now on the rise amongst deer in some parts of the U.S., can be transmitted to humans or not. Test tube studies like this one might help answer that question, and– in the case that the deer prions can make the leap—such studies may inform scientists about what those prions might look like, he said. By studying any new prion strains created in mice with the human prion protein, scientists might also gain insight into the potential symptoms associated with those diseases. ” The data demonstrate that PMCA is a valuable tool for the investigation of the strength of the barrier between diverse species, its molecular determinants, and the expected features of the new infectious material produced,” the researchers concluded. “Finally, our findings suggest that the universe of possible prions is not restricted to those currently known but that likely many unique infectious foldings of the prion protein may be produced and that one of the sources for this is cross-species transmission.” This research makes it extremely clear that there is an inherent risk in feeding one species to another. As prions are believed to be able to cross the blood brain barrier, if you eat an animal that has infectious prions, even if those prions are not capable in and of themselves of infecting you, there is a risk that they will interact with your own prions to create a whole new variety of infectious prion protein that CAN harm us. Perhaps this is how Creutzfeldt-Jakob disease originated. The sensible thing to do is to take great care in ensuring our food animals are free of prion disease, all the way down their food chain. Cattle feed is often surprisingly high in animal protein. Feeding animal protein to herbivores seems to me to be an entirely unnecessary risk factor in disease transmission. Equally, just because a prion disease is not known to be transferable in the traditional sense, does not mean that we should be eating infected deer or rabbits. The North Carolina Department of Agriculture has a handy guide for removing all the parts of a deer that are especially high in prions. Another major plus involved in contracting the clean-up effort of your home with a professional service is the wide range of jobs they are able to service. People should feel like they have learned something from your articles and they should want to click on the links you provide. The best way to do this I feel is to use a synergistic blend of plants that help your body produce the proper harmonious hormone balance. The stormwater fee can be found on quarterly water bills and is based on the amount of impervious surfaces on a property. At Vision Forum, we are dedicated to the restoration of Christian family culture. If doing this on your own, be sure to apply a carpet disinfectant as soon as possible. Chickenpox usually occurs in childhood, is one of childhood diseases. At the age of adult Varicella virus usually causes a rash localized to one or more dermatomes, known as herpes zoster or shingles, hence the name of the Varicella-zoster virus. Chickenpox is a classic disease of childhood, which usually is easy for children but for teenagers and adults may have an increased risk of complications. The disease can take about a week. Chickenpox in children is characterized by a very aggressive rash which occurs in waves, it includes several areas of the body, starting in early stages, with head; chickenpox is a form of viral infection, caused by the Varicella-zoster, which is part of the family Herpesviridae. Varicella infection is a very contagious condition; sick child is the main source of infection for other children in that school communities, kinder gardens, and nursery. Child with Varicella (chickenpox) can easily contaminate other children, especially in the first 2-3 days after onset, before actual clinical onset of disease, when symptoms are almost unnoticeable. Contamination can be done directly, by touching contaminated areas and liquid vesicles that appear on the skin or by respiratory secretions, which also contain the virus. Time after the eruption, usually must isolate sick child at home for 14 days to heal and to avoid infection of other children. The incubation period for chickenpox is about 15 days, the child does not show many symptoms, apart from feeling bad and tiredness. Follow pre-eruptive period, characterized by mild fever, headaches and other muscle pain, followed closely by eruptive period, which covers up to 10 days. During this time a rash appears, nearly always accompanied by fever and the child becomes agitated. The first elements of rash appear on the body, and then extend the head and limbs, most finding it on the trunk, the arm and thrust. But they also appear on the face, hairy skin of the head and hands. Symptoms of chickenpox - Fatigue and irritability for 1 or 2 days before rash manifestation - Characteristic skin rash and itching on the trunk, under the arms, on the face, limbs, mouth and sometimes the trachea and bronchial tubes. - Fever, general malaise - Loss of appetite - Muscle pain and / or joints - Cough, runny nose The chickenpox symptoms resemble those of other diseases, so you should see your doctor for diagnosis. What are we doing in case of chickenpox in children? In children is usually enough to take general measures to improve symptoms. For fever is administered paracetamol or ibuprofen, always avoiding aspirin (acetylsalicylic acid), whose use for Varicella is associated with complications. Itching can be treated with oral antihistamines or antipruritic lotions. Other measures that can be taken to avoid skin damage caused by scratching are totally cut nails and a daily bath with shampoo with neutral PH. General treatment in case of Varicella or chickenpox consists of bed rest and light diet, lacto-flour-sugar, in fever period. Fever can be controlled with aspirin (in adults) and paracetamol. It should be given special attention to hygiene skin and mucous membranes to avoid vesicle infection. Child must not scratch, this causing other bacterial infections. Nails should be cut to reduce the effectiveness of scratch. It is indicated to use powder the skin with mint talc. Natural treatment for chickenpox with Calivita products - Beta Carotene is effective in immune system consolidation and in reducing symptoms in dermal diseases such as acne, scabies, shingles, psoriasis, vitiligo, lupus erythematosus, mycosis of the skin and eruptive diseases (measles, chickenpox). - Bee Power has the quality to enhance the immune system function due to the richness in nutrients and bactericidal effect. Increase the capacity of the defense against microbial and infectious diseases. - Full Spectrum is a complex of vitamins and minerals that strengthen the immune system, enhances physical and mental strength and helps prevent infectious diseases. - C Plus contains a combination of Vitamin C and bioflavonoids for the best effect.
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The control system for controlling the speed of a turbine or other rotating member typically includes means for providing a setpoint or reference signal that represents the desired rotational speed. A servo circuit compares the setpoint signal with a feedback signal representing the actual speed to produce an error signal that is used to minimize the difference between the setpoint and actual speeds. Although for some applications a setpoint controller could simply comprise a potentiometer, there are many applications for which a more precise and versatile method of controlling the setpoint is required. For example, during testing of a propeller turbine drive, it may be required to rotate the propeller at a known rate for a prescribed time period, then accelerate the propeller to a second known rate at a prescribed ramping (i.e., acceleration) rate, etc. In carrying out such a program, the convenience and versatility of the setpoint controller can be a significant factor in minimizing testing time, an important consideration during wind tunnel testing in which the on-line testing time is limited and expensive. An even more demanding application for a setpoint controller is one in which the speed of two related elements must be controlled. An example of such an application is wind tunnel testing of a twin turbine counter-rotating propeller system for a jet aircraft engine. To test such a system, it is necessary to rapidly cycle between different speed levels for the different propellers, and to provide means for precisely establishing the relative speeds and relative acceleration or decelerations of the individual propellers. No prior setpoint controller or controller systems have been found adequate to efficiently test such a system.
3.03125
3
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Q: What is the first recorded observation of Good Friday? When was the first Good Friday commemoration observed, distinct from Pascha/Passover or Sunday Easter? Related: What is the origin of the Good Friday tradition? However, I am not interested in when or where the idea of it being Friday came from, but simply what and when the first record of a "Good Friday" was. A: The Didascalia Apostolorum, dated to AD 230, prescribe activities during Holy Week, including a fast on Friday: Therefore you shall fast in the days of the Pascha from the tenth, which is the second day of the week; and you shall sustain yourselves with bread and salt and water only, at the ninth hour, until the fifth day of the week. But on the Friday and on the Sabbath fast wholly, and taste nothing. [v. 19] You shall come together and watch and keep vigil all the night with prayers and intercessions, and with reading of the Prophets, and with the Gospel and with Psalms, with fear and trembling and with earnest supplication, until the third hour in the night after the Sabbath; and then break your fasts. (v18–19) Something similar is related in the Apostolic Constitutions (dated to 375–380) for Friday, the sixth day of the week: But He commanded us to fast on the fourth and sixth days of the week; the former on account of His being betrayed, and the latter on account of His passion. But He appointed us to break our fast on the seventh day at the cock-crowing, but to fast on the Sabbath-day. Not that the Sabbath-day is a day of fasting, being the rest from the creation, but because we ought to fast on this one Sabbath only, while on this day the Creator was under the earth. (5.3.15) The Pilgrimage of Etheria (or Egeria), dated to a few years later, describes a more elaborate celebration, with five main stages: Service at daybreak "And when they arrive before the Cross the daylight is already growing bright." Column of the flagellation "they all go at once with fervour to Sion, to pray at the column at which the Lord was scourged." Veneration of the cross "The casket is opened and (the wood) is taken out, and both the wood of the Cross and the title1 are placed upon the table. Now, when it has been put upon the table, the bishop, as he sits, holds the extremities of the sacred wood firmly in his hands, while the deacons who stand around guard it." Station before the cross "Thus from the sixth to the ninth hours the lessons are so read and the hymns said, that it may be shown to all the people that whatsoever the prophets foretold of the Lord's Passion is proved from the Gospels and from the writings of the Apostles to have been fulfilled." Evening offices "And after the dismissal at the martyrium, they go to the Anastasis, where, when they arrive, the passage from the Gospel is read where Joseph begged the Body of the Lord from Pilate and laid it in a new sepulchre." The excerpts above are taken from the full text of The Pilgrimage of Etheria, which is too lengthy to quote here in full. The Encyclopedia of Ancient Christianity briefly summarizes: Christians spent the time reflecting upon Jesus’ morning appearance before Pilate (Mk 15:2-15 and parallel texts) and the flagellation (Mk 15:16-20 and parallel texts). At noon, the wood of the cross found by Helena was shown to the faithful; then, for three hours, the people read the account of the passion, along with OT prophecies about Christ.
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Remote evaluation In computer science, remote evaluation is a general term for any technology that involves the transmission of executable software code from a client computer to a server computer for subsequent execution at the server. After the code has finished executing, the results of its execution are sent back to the client. Remote evaluation belongs to the family of mobile code, within the field of code mobility. An example for remote evaluation is grid computing: An executable task may be sent to a specific computer in the grid. After the execution has terminated, the result is sent back to the client. The client in turn may have to reassemble the different results of multiple concurrently calculated subtasks into one single result. See also Client-side scripting, the client executing code sent by the server, instead of the server executing code sent by the client Code on demand Code mobility Category:Grid computing Category:Evaluation strategy
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Geneticists hope to unlock secrets of bats’ complex sounds November 18, 2016This article courtesy of Nature News. Project to sequence the DNA of more than 1,000 species seeks to reveal how bats learn to communicate. Some bats sing or call just as birds and humans do. But how they learn their calls and melodies is a mystery — one that scientists will try to solve by sequencing the genomes of more than 1,000 bat species. The project, called Bat 1K, was announced on 14 November at the annual meeting of the Society for Neuroscience in San Diego, California. Its organizers also hope to learn more about the flying mammals’ ability to navigate in the dark through echolocation, their strong immune systems that can shrug off Ebola and their relatively long lifespans. “The genomes of all these other species, like birds and mice, are well-understood,” says Sonja Vernes, a neurogeneticist at the Max Planck Institute for Psycholinguistics in Nijmegen, the Netherlands, and co-director of the project. “But we don’t know anything about bat genes yet.” Some bats show babbling behaviour, including barks, chatter, screeches, whistles and trills, says Mirjam Knörnschild, a behavioural ecologist at Free University Berlin, Germany. Young bats learn the songs and other sounds from older male tutors. They use these sounds during courtship and mating, when they retrieve food and as they defend their territory against rivals. Scientists have studied the vocal sounds of only about 50 bat species so far, Knörnschild says, and they know much less about bat communication than about birds’. Four species of bats have so far been found to learn vocal sounds from each other, their fathers and other adult males, just as a child gradually learns how to speak from its parents. The four species are: the greater sac-winged bats (Saccopteryx bilineata), the Egyptian fruit bat (Rousettus aegyptiacus), the pale spear-nosed bat (Phyllostomus discolor) and the greater spear-nosed bat (Phyllostomus hastatus). The bats exhibit diversity in their geographic locations, gender and age of vocalizing and frequency and types of sounds. Winged singers Genetic studies have identified at least one gene in bats that is linked to speech and language, called FOXP2. The gene is also known to have a role in how people learn language, and in vocal learning in songbirds. The versions of FOXP2 found in these species are often very similar, but bats are an exception. FOXP2 seems to have evolved to be much more diverse in bats than in people, Knörnschild says. The reason why is a mystery. Researchers working on the Bat 1K project expect to find that other genes are also involved in communication, and that many more bat species have the ability to learn songs, calls or other sounds. “It's not a rare trait,” Knörnschild says. “I'm becoming convinced that there’s a whole continuum in bat vocal learning, and it’s more widespread than just four species.” Bats’ echolocation ability has been studied for many years, partly because of its applications to sonar and radar. But scientists know very little about the acoustic communication and social behaviour that drive how bats learn their songs and sounds, says Michael Yartsev, a neurobiologist at University of California, Berkeley. The study of vocal learning in bats is “nearly completely untapped”, he says — likening it to the state of research into birdsong 60 years ago. Songbirds have been studied in detail, especially the zebra finch (Taeniopygia guttata), which is easy to breed in a lab, says Tecumseh Fitch, a cognitive biologist at the University of Vienna. But birds don’t have a mammalian brain or use a larynx to make sounds. Some mammals, including elephants, whales, pinnipeds and dolphins, display vocal learning, but bats are much more practical to study. “My hope is that bats will become the model species for vocal learning,” Fitch says.
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Mandarin Chinese in the Philippines Mandarin Chinese is spoken and taught academically to Chinese Filipinos in the Philippines. Both Standard Chinese and Taiwanese Mandarin are taught and spoken in the Philippines, with some schools and speakers using Simplified Chinese characters, some using Traditional Chinese characters, and some using a mixture of both. Classification Mandarin in the Philippines can be classified into two distinct Mandarin dialects: Standard Mandarin and Colloquial Mandarin. Standard Mandarin is either the standard languages of Mainland China and Taiwan, while Colloquial Mandarin in the Philippines tends to combine features from Mandarin () and features from Hokkien () of the local Philippine Hokkien dialect, which is the heritage language of many Chinese Filipinos. Usage Only a small minority of Chinese Filipinos claim Mandarin as their native first language, with Tagalog or English typically being the first language. The lack of environment for speaking the language and the difficulty of learning it created not just a lack of interest, but even great disgust by some towards it. Efforts in the 21st century to promote Mandarin Chinese education in Chinese Filipino institutions and recent utilitarian trends, such as more Mandarin job opportunities, recent immigrants from China or Taiwan, summer education trips to China or Taiwan, encouragement of universities and schools by past presidents, and education exchange deals with China have spurred interest and potential for growth in the usage of Mandarin. Code-switching Sometimes Chinese Filipinos also code-switch Mandarin together with other languages, such as English, Tagalog (or other Philippine languages), and Hokkien, as a form of pidgin language, just like Hokaglish or Singlish. Education In terms of phonology, vocabulary and grammar, the Mandarin taught in the Philippines is often the Taiwanese variety ("Guóyǔ") of Standard Chinese because many Chinese Filipino schools use dictionaries and books from Taiwan. In recent years, some have also began using books and teaching materials from Mainland China, Singapore, and Malaysia. Filipino Mandarin newspapers use the Traditional Chinese characters in writing. Due to selection of founders and sponsors of Chinese schools, schools either teach using only Simplified Chinese characters, only Traditional Chinese characters, or a mixture of both. 'Many Chinese Filipino schools use pinyin or bopomofo (zhuyin fuhao) to teach the language. Chinese Filipino schools often use the first language approach, which assumes that students of Chinese Filipino schools have had native experience of Mandarin. See also Philippine Hokkien Languages of Philippines References Category:Chinese-Filipino culture Category:Mandarin Chinese *
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Multiple challenges remain to Fukushima nuclear cleanup by Mari Yamaguchi This Sept. 4, 2017 aerial photo shows Fukushima Dai-ichi nuclear power plant reactors, from bottom at right, Unit 1, Unit 2 and Unit 3, in Okuma, Fukushima Prefecture, northeastern Japan. The three reactors that had meltdowns together have 1,573 units of mostly used nuclear fuel rods that are still inside and must be kept cool in pools of water. They are considered among the highest risks in the event of another major earthquake, because the pools are uncovered. The plant operator, Tokyo Electric Power Co. or TEPCO, plans to begin removing the rods from reactor unit 3 in the fiscal year beginning next April 1. However, the latest roadmap delays removal of the rods from units 1 and 2 for three years until fiscal 2023, because further decontamination work and additional safety measures are needed. (Daisuke Suzuki/Kyodo News via AP) Japan's government approved a revised road map Tuesday to clean up the radioactive mess left at the Fukushima nuclear power plant after it was damaged beyond repair by an earthquake and tsunami in 2011. Decommissioning the damaged reactors is an uncertain process that is expected to take 30 to 40 years. A look at some of the challenges: ___ THE FUEL RODS The three reactors that had meltdowns together have 1,573 units of mostly used nuclear fuel rods that are still inside and must be kept cool in pools of water. They are considered among the highest risks in the event of another major earthquake that could trigger fuel rods to melt and release massive radiation due to loss of water from sloshing or structural damage because the pools are uncovered. The plant operator, Tokyo Electric Power Co., or TEPCO, plans to begin moving the rods from reactor Unit 3 in the fiscal year beginning April 1. However, the latest road map delays removal of the rods from units 1 and 2 for three years until fiscal 2023, because further decontamination work and additional safety measures are needed. Ironically, because the building housing reactor 3 was more heavily damaged, it is easier to remove that unit's fuel rods. The fuel rods will be moved to a storage pool outside the reactors, and eventually sent for long-term storage in what are known as dry casks. In this Nov. 12, 2014 file photo, a Tokyo Electric Power Co. (TEPCO) official wearing a radioactive protective gear stands in front of Advanced Liquid Processing Systems during a press tour at the Fukushima Dai-ichi nuclear power plant in Okuma, Fukushima Prefecture, northeastern Japan. Japan's government approved a revised roadmap Tuesday, Sept.26, 2017, to clean up the radioactive mess left at the Fukushima nuclear power plant after it was damaged beyond repair by an earthquake and tsunami in 2011. Decommissioning the damaged reactors is an uncertain process that is expected to take 30 to 40 years. (AP Photo/Shizuo Kambayashi, Pool, File) ___ THE MELTED FUEL By far the hardest part of decommissioning Fukushima will be removing the fuel that melted and presumably spilled out of the reactor cores. In July, an underwater robot for the first time captured images inside the primary containment chamber of Unit 3. They showed a large number of solidified lava-like rocks and lumps on the chamber's floor, believed to be melted fuel mixed with melted and mangled equipment and parts of the structure. The search for melted fuel in units 1 and 2 has so far been unsuccessful. The water level is lower, so crawling robots have been tried, but they have been obstructed by debris as well as extremely high radiation levels. Despite the unknowns about the melted fuel and debris and their whereabouts, the road map calls for finalizing the removal method in 2019, and starting actual removal at one of the reactors in 2021. The government-funded International Research Institute for Nuclear Decommissioning is developing robots and other technology to carry out the work. ___ In this July 21, 2017 file photo, this image captured by an underwater robot provided by International Research Institute for Nuclear Decommissioning shows lava-like lumps believed to contain melted fuel inside the Unit 3 reactor at Fukushima Dai-ichi nuclear plant in Okuma town, northeastern Japan. Japan's government approved a revised roadmap Tuesday, Sept.26, 2017, to clean up the radioactive mess left at the Fukushima nuclear power plant after it was damaged beyond repair by an earthquake and tsunami in 2011. Decommissioning the damaged reactors is an uncertain process that is expected to take 30 to 40 years. (International Research Institute for Nuclear Decommissioning via AP, File) CONTAMINATED WATER TEPCO has treated and stored a massive amount of radioactive water—about 800,000 tons—and the volume is growing every day. Cooling water leaks out of the damaged reactors and mixes with groundwater that seeps into the basements of the reactor building, increasing the amount of contaminated water. The utility has managed to halve the volume to 200 tons per day by pumping up groundwater via dozens of wells dug upstream from the reactors, as well as installing a costly "ice wall" by freezing the ground to block some of the water from coming in and going out. The water is stored in hundreds of tanks that cover much of the plant property. They get in the way of decommissioning work and pose another risk if they were to spill out their contents in another major earthquake or tsunami. After treatment, the water still contains radioactive tritium, which cannot be removed but is not considered harmful in small amounts. Experts say controlled release of the water into the ocean is the only realistic option, but TEPCO has not moved forward with that plan because of opposition from fishermen and residents who fear a negative image and possible health impact. ___ RADIOACTIVE WASTE In this Nov. 12, 2014 file photo, workers wearing protective gears stand on the water tank containing contaminated water that has been treated at the Fukushima Dai-ichi nuclear power plant in Okuma, Fukushima prefecture, northeastern Japan. Japan's government approved a revised roadmap Tuesday, Sept. 26, 2017, to clean up the radioactive mess left at the Fukushima nuclear power plant after it was damaged beyond repair by an earthquake and tsunami in 2011. Decommissioning the damaged reactors is an uncertain process that is expected to take 30 to 40 years. (AP Photo/Shizuo Kambayashi, Pool, File) Japan has yet to develop a plan to dispose of the highly radioactive waste that will come out of the Fukushima reactors. Under the road map, the government and TEPCO will compile a basic plan during fiscal 2018. Managing the waste will require new technologies to compact it and reduce its toxicity. Finding a storage site for the waste seems virtually impossible, as the government has not been able to find a site even for the normal radioactive waste from its nuclear power plants. The prospect raises doubts about whether the cleanup can really be completed within 40 years. This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only. User comments There is no melted fuel to be located today. The material in the photograph is believed to be solidified material (corium) which was formed in March, 2011, when fuel melted and mixed with other materials in the reactor. Where ever this material is now, it has cooled to a temperature near room temperature. Most of the radioactive isotopes have been removed from the stored water. The remnant is tritium, which is a weak beta emitter. E-mail the story Multiple challenges remain to Fukushima nuclear cleanup Note Your email address is used only to let the recipient know who sent the email. Neither your address nor the recipient's address will be used for any other purpose. The information you enter will appear in your e-mail message and is not retained by Phys.org in any form. Your message Newsletter sign up Get weekly and/or daily updates delivered to your inbox. You can unsubscribe at any time and we'll never share your details to third parties. 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